2- ethanol 3-Ethoxyethyl acetate

Ethanol, 2-methoxy-, 62 Ethanolamines, 62 Ethmylestradiol, 62 Ethion, 62 Ethoprophos, 63 2-Ethoxyethanol, 63 2-Ethoxyethyl acetate, 63 Ethyl acetates, 63 Ethyl acetylene, 63... 

Methylethoxy)ethanol 2-(2-Butoxyethoxy)-ethanol acetate/Diethylene glycol n-butyl ether acetate 2-(2-Butoxyethoxy)-ethanol 2-(2-Ethoxyethoxy)ethanol 2-(2-ethoxyethoxy)ethyl acetate 2-(Butoxyethoxy)ethyl acetate 2-Butanol 2-Butanone 2-Butoxyethanol 2-Butoxyethyl acetate 2-Ethoxyethanol 2-Ethoxyethyl acetate 2-Ethylhexane-1,3-diol 2-Ethylhexanol... 

Ethoxyethanol) see Ethyl glycol (2-(2-Ethoxyethoxy)ethanol) see Ethyldiglycol (2-Ethoxyethyl acetate) see Ethyl glycol acetate... 

A subsequent elimination of hydrogen halide prompted by the lability of halogen on the carbon attached to nitrogen, a second halogen addition, and a repetition of the cycle must account for the reported formation of 9-pentachloro- and 9-pentabromoethylcarbazoles on reaction with excess halogen in methanol and acetic acid, respectively. Addition of bromine to IV-vinylcarbazole in benzene as solvent was accompanied by 3,6-dibromi-nation in ethanol, 3,6-dibromo-9-(2-bromo-l-ethoxyethyl)carbazole was reportedly formed (cf. ref. 230). 

Ethane, 1-bromo-2-ethoxy-, 23, 32 Ethanolamine, 26, 38 Ethanol, 2-isopropylamino-, 26, 38 Ether, anhydrous, 22, 57 Ether, butyl o-nitrophenyl, 25, 9 /3-Ethoxyethyl alcohol, 23, 32 /3-Ethoxyethyl bromide, 23, 32, 33 /3-Ethoxyethyl cyanide, 23, 33 Ethoxymagnesiomalonic ester, 25, 73 2-Ethoxy-1-naphthaldehyde, 20,11 6-Ethoxy-8-nitroquinoline, 27, 52 /3-Ethoxypropionaldehyde acetal,... 

Irradiation at 254 nm in the charge-transfer band of the complex between diethyl ether and oxygen leads to several products (with the quantum yields given) H2Oa (0.24), 1-ethoxyethyl hydroperoxide (0.04), ethyl acetate (0.26), acetaldehyde (0.18), ethanol (0.18), ethyl formate (0.04), methanol (0.035), formaldehyde (0.005), and ethyl vinyl ether (0.013).197 The primary process appears to be electron transfer from ether to oxygen, as shown in reaction (37). Reaction with... 

The synthesis of nonracemic a,P-unsaturated sulfoxides bearing an electron-withdrawing group at the a-position has received attention [28-30] because these types of substrates have proved useful as chiral dienophiles (see Section 5.5) [28,29]. These methods suffered from the disadvantage that several steps were involved. Maignan and coworkers [31] have recently described a one-pot synthesis of nonracemic a-acyl- and a-hydroxyalkyl-a,P-unsaturated sulfoxides from 2-ethoxyethyl p-tolyl sulfoxide (16), readily prepared from (/ )-p-tolyl vinyl sulfoxide by addition of sodium ethoxide in ethanol. Thus, treatment of (16) with LDA in THF, followed by the addition of ethyl acetate, gave enantiomerically pure a-acyl-a,P-unsaturated sulfoxide (18) in 69% yield via the intermediate (17) (Scheme 5.6). 

Ethoxyethylperoxyls were prepared by a variety of methods and react to give ethyl acetate, ethanol, acetaldehyde and ethyl formate. (Table V). There was no evidence for the formation of di-(1-ethoxyethyl) peroxide, a result that is not entirely incompatible with Diaper s work in view of the large difference in the size the peroxy radicals studied by the two groups of workers. The absolute yields of the products were difficult to ascertain with any degree of certainty because of secondary reactions. The high yield of ethyl formate is, however, diagnostic for the intermediacy of alkoxy radicals and indicates that at least 20 of the self-reactions of 1-ethoxyethylperoxyls occur via the radical mechanism. 

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