Ethers, cleavage tetrahydropyranyl

Hydrolysis of cyclic orthoesters Ozonolysis of tetrahydropyranyl ethers Cleavage of vinyl orthoesters... 

Cleavage of tetrahydropyranyl ethers.16 Tetrahydropyranyl ethers are cleaved to the alcohol by dimethylaluminum chloride or methylaluminum dichloride in high yield at temperatures of -25 to 25°, conditions that do not affect f-butyldimethylsilyl ethers. MOM and MEM ethers are converted into ethyl ethers by a methyl transfer reaction. 

Protection and deprotection. Tetrahydropyranyl ether cleavage is catalyzed by CAN at pH 8. Acetonides are formed from diols under the influence of CAN. ... 

Ether cleavage. The polymer-bound reagent catalyzes hydrolysis of TBS ether and acetals in aqueous acetonitrile. Methoxymethyl and tetrahydropyranyl ethers are stable under such conditions. 

The principal variations on the normal crown synthesis methods were applied in preparing mixed crowns such as those shown in Eq. (3.55) and in forming isomers of the dibinaphthyl-22-crown-6 systems. The latter has been discussed in Sect. 3.5 (see Eq. 3.21) . The binaphthyl unit was prepared to receive a non-naphthyl unit as shown in Eq. (3.57). Binaphthol was allowed to react with the tetrahydropyranyl ether or 2-chloroethoxyethanol. Cleavage of the THP protecting group followed by tosyla-tion of the free hydroxyl afforded a two-armed binaphthyl unit which could serve as an electrophile in the cyclization with catechol. Obviously, the reaction could be accomplished in the opposite direction, beginning with catechol". ... 

Using day supported ammonium nitrate (dayan), selective deprotection of methoxyphenyl methyl (MPM) ether has been achieved recently using microwave irradiation in solvent-free conditions (Scheme 6.15) [56]. The same reagent has been used for the cleavage of tetrahydropyranyl (THP) ethers. A similar selective preparation and deavage of THP ethers has been achieved under microwave irradiation catalyzed by iodine [57] or neat reaction in an ionic liquid [28],... 

Sulfur analogs, 2-tetrahydrofuranyl and 2-tetrahydropyranyl thioethers, were reduced by alone to alkyl 4- or alkyl 5-hydroxyalkyl thioethers resulting from the preferential reductive cleavage of the carbon-oxygen (rather than the carbon-sulfur) bond. Thus refluxing for 2 hours with alane in ether converted 2-alkylthiotetrahydrofurans to alkyl 4-hydroxybutyl thioethers in 63-72% yields, and 2-alkylthiotetrahydropyrans to alkyl 5-hydroxypentyl thioethers in 58-82% yields [794]. 

Alkyl tetrahydropyranyl ethers (118 R = Et or Bu) behave similarly (68JOC2266). In both cases, the base peak occurs at m/e 85, resulting from loss of an RO radical from [M]t. Pathways which involve ring cleavage of the molecular ion are also operative and appear to be of greater importance.for the ethyl ether (118 R = Et). 

Tetrahydropyranyl (THP) ethers, another species known to be unstable to acid, have similarly been reported to be cleaved by solutions of iodine in methanol.209 At room temperature, cleavage of the THP ethers was complete in 1.5 to 8 h. As with the previous example using iodine in methanol at lower than reflux temperature, TBDMS ethers were stable to these conditions. The ability to tune the reactivity of the iodine in methanol system by simply controlling the temperature is of value in selective deprotection. This is even more useful when fluorine, known to remove only silyl ethers,105 is exploited. Given that methoxymethyl ethers, essentially acetals, are known to be cleaved under acidic conditions, it seems likely they too should be subject to removal by solutions of iodine in methanol. Sundry examples of deprotections using iodine in methanol are presented in Table IV. 

Cleavage of acid-labile protective groups.1 The reaction of H202 (70%, FMC) and CI3CCOOH in CH2C12/(-butyl alcohol converts a dimethyl acetal (1) into a hydroperoxy methyl acetal (a), which can be isolated but which for convenience (and safety) is reduced to the aldehyde 2 in 80% overall yield. The same conditions can effect oxidative cleavage of tetrahydropyranyl and trityl ethers. 

One method that has found widespread use for the protection of an alcohol is reaction with dihydropyran to form a tetrahydropyranyl ether. Once the desired reaction has been accomplished, the protecting group can be removed by treatment with aqueous acid or acid and ethanol. The formation of a tetrahydropyranyl ether and its cleavage are illustrated in the following equation ... 

The mechanism of the formation of the tetrahydropyranyl ether (see Figure 23.1) is an acid-catalyzed addition of the alcohol to the double bond of the dihydropyran and is quite similar to the acid-catalyzed hydration of an alkene described in Section 11.3. Dihydropyran is especially reactive toward such an addition because the oxygen helps stabilize the carbocation that is initially produced in the reaction. The tetrahydropyranyl ether is inert toward bases and nucleophiles and serves to protect the alcohol from reagents with these properties. Although normal ethers are difficult to cleave, a tetrahydropyranyl ether is actually an acetal, and as such, it is readily cleaved under acidic conditions. (The mechanism for this cleavage is the reverse of that for acetal formation, shown in Figure 18.5 on page 776.)... 

Our final example is a base-labile 4-(phenylsulfonyl)methyl-l,3-dioxolane protecting group for aldehydes and ketones.4 Protection is carried out by the reaction of diol 17,1 (obtained by dihydroxylation of ally phenyl sulfone) with a carbonyl compound in the presence of pyridinium p-toluene sulfonate [Scheme 2.17], Cleavage is accomplished by treatment with DBU. /erf-Butyldimethylsilyl ethers, p-toluenesulfonate esters, tetrahydropyranyl ethers, carboxylic esters and benzoates are well tolerated. A disadvantage to the use of 17.1 is the introduc-... 

Recent methods for the cleavage of allyl ethers that have that have yet to be tested on the anvil of complex target synthesis include (a) diborane generated in situ by reaction of sodium borohydride with iodine in THF at 0 °C (cyanoT ester, nitro, acetonide and tetrahydropyranyl groups survive) 434 (b) cerium(Ill) chloride and sodium iodide in refluxing acetonitrile (benzyl. THP and Boc groups survive) 435 (c) iodotrimethylsilane in acetonitrile at room temperature 436 and (d) DDO in wet dichloromethane (secondary allyl ethers, benzyl, acetate and TBS groups survive).437... 

This procedure consists of the synthesis of a precursor, methoxymethyl vinyl ether, an a-hydroxy enol ether, and the intramolecular hydrosilylatlon of the latter followed by oxidative cleavage of the silicon-carbon bonds. The first step, methoxymethylation of 2-bromoethanol, is based on Fujita s method.7 The second and third steps are modifications of results reported by McDougal and his co-workers. Dehydrobromination of 2-bromoethyl methoxymethyl ether to methoxymethyl vinyl ether was achieved most efficiently with potassium hydroxide pellets -9 rather than with potassium tert-butoxide as originally reported for dehydrobromination of the tetrahydropyranyl analog.10 Potassium tert-butoxide was effective for the dehydrobromination, but formed an adduct of tert-butyl alcohol with the vinyl ether as a by-product in substantial amounts. Methoxymethyl vinyl ether is lithiated efficiently with sec-butyllithium in THF and, somewhat less efficiently, with n-butyllithium in tetrahydrofuran. Since lithiation of simple vinyl ethers such as ethyl vinyl ether requires tert-butyllithium,11 metalation may be assisted by the methoxymethoxy group in the present case. 

Table S Cleavage of Tetrahydrofuranyl and Tetrahydropyranyl Ethers with HAlCh and with LiAlH4 BF3...

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