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1.5- dimethyl-2-hydroxymethyl

Aus Pyridoxal wird unter Erhalt der Alkohol-Gruppe 3-Hydroxy-2,4-dimethyl-5-hydroxymethyl-pyridin erhalten (s.a. S. 628)12 ... [Pg.604]

Chromanone, 3-acetamido-2-methyl-reduction, 3, 729 Chromanone, 3-amino-synthesis, 3, 734 Chromanone, 3-arylidene-thermoisomerization, 3, 722 Chromanone, 3-benzylidene-thermolysis, 3, 728 Chromanone, 3-bromo-2-hydroxy-benzofuran from, 3, 729 Chromanone, 6,8-dimethyl-hydroxymethylation, 3, 731 Chromanone, 2,3-epoxy-as synthon, 3, 735... [Pg.579]

Phenol 2-Trimethylsilyl- XIII/5, 42 Silan Dimethyl-hydroxymethyl-phenyl- XIII/5, 74... [Pg.650]

Propylene Urea Resins. In similat fashion to ethyleneurea, dimethyl-olpropyleneurea [3270-74-4] [l,3-bis(hydroxymethyl)tetrahydro-2-(m)-pyrimidinone] is the basis of propyleneurea—formaldehyde resin [65405-39-2], Its preparation is from urea, 1,3-diaminoptopane [109-76-2] and formaldehyde. [Pg.329]

In some instances the solvents may react with the substrate during the irradiation. For example, 3,6-dichIoropyridazine, when irradiated in acidified methanol, gives a mixture of raonoraethylated (56), dimethylated (57) and hydroxyraethylated (58) compounds. Further transformation of the hydroxymethyl compound (58) results in the formation of y-Iactones (59) and succinates (60 Scheme 20). [Pg.14]

The concept and use of free radical attack on pyrimidines has been little developed. However, pyrimidine does react slowly with p-nitrobenzenediazonium chloride to yield some 2- and 4-p-nitrophenylpyrimidines (51JCS2323) in addition, 2,4-and 4,6-dimethyl-pyrimidine are converted by hydroxymethylene radicals (from ammonium peroxydisul-fate/methanol) into 6- and 2-hydroxymethyl derivatives, respectively (77H(6)525). Certain bipyrimidine photoproducts appear to be formed from two similar or dissimilar pyrimidinyl radicals (see Section 2.13.2.1.4). [Pg.73]

Indole, 3-hydroxymethyl-2-phenyl-stability, 4, 272 Indole, I-hydroxy-2-phenyl-synthesis, 4, 363 Indole, 2-iodo-synthesis, 4, 216 Indole, 3-iodo-reaetions, 4, 307 synthesis, 4, 216 Indole, 2-iodo-l-methyl-reaetions, 4, 307 Indole, 2-lithio-synthesis, 4, 308 Indole, 3-lithio-synthesis, 4, 308 Indole, 2-mereapto-tautomerism, 4, 38, 199 Indole, 3-mercapto-tautomerism, 4, 38, 199 Indole, 3-methoxy-synthesis, 4, 367 Indole, 5-methoxy-oxidation, 4, 248 Indole, 7-methoxy-2,3-dimethyl-aeetylation, 4, 219 benzoylation, 4, 219 Indole, 5-methoxy-l-methyl-reduetion, 4, 256 Indole, 5-methoxy-l-methyl-3-(2-dimethylaminoethyl)-reaetions... [Pg.668]

Pterin, 5-formyl-6,7-dimethyl-5,6,7,8-tetrahydro-structure, 3, 281 Pterin, 6-hydroxymethyl-reactions, 3, 304 structure, 3, 273 Pterin, 7-hydroxymethyl-synthesis, 3, 311... [Pg.756]

Pterin, 6-hydroxymethyl-7,7-dimethyl-7,8-dihydro-bacteriostatic activity, 3, 325 Pterin, 1-methyl-hydrolysis, 3, 294 5-oxide... [Pg.756]

Dimethyl peroxide Diethyl peroxide Di-t-butyl-di-peroxyphthalate Difuroyl peroxide Dibenzoyl peroxide Dimeric ethylidene peroxide Dimeric acetone peroxide Dimeric cyclohexanone peroxide Diozonide of phorone Dimethyl ketone peroxide Ethyl hydroperoxide Ethylene ozonide Hydroxymethyl methyl peroxide Hydroxymethyl hydroperoxide... [Pg.238]

Demethylation of trequinsin (3) with a 65 35 mixture of AcOH and 48% HBr at 115 °C for 3 h gave mainly 10-hydroxyl derivatives 148 (R = r = H), which was accompanied by traces of its 9-hydroxyl and 9,10-dihydroxy derivatives. In boiling 48% HBr for 2 h its 9,10-dihydroxy derivative formed in 63% yield (98IJC(B)1). 9-Methoxy group of 3 and that of its 2-[(2,6-dimethyl-4-carboxyphenyl)imino] derivative 178 (R = COOH) was selectively demethylated by the treatment with 60% NaOH and EtSH in HMPA. Treatment of 3 with pyridine HCl in boiling pyridine for 20 min afforded its 9,10-dihydroxy-3-desmethyl derivative in 65% yield. 4 -Hydroxymethyl... [Pg.255]

Dimethyl-4-hydroxymethyl-1.3-dioxolane Sodium hydride Hydrogen chloride... [Pg.645]

Step G 4-fOrtho-(2, 3 -Dihydroxypropyloxycarbonyl)-Phenyl]-Amino-8-Trifluoromethyl-quinoHne Acetonide — 100 cc of toluene were added to 80 cc of 2,2-dimethyl-4-hydroxy-methyl-1,3-dioxolane and the toluene was distilled off under reduced pressure to eliminate the water present. To the anhydrous 2,2-dimethyl-4-hydroxymethyl-1,3-dioxolane thus obtained, 0.25 gram of an oily 50% suspension of sodium hydride and then 21.3 grams of 4-... [Pg.646]

Chemical Name 3-Pyridine carboxylic acid compounded with 3,7-dihydro-7-[2-hydroxy-3-[(2-hydroxymethyl)methylamino] propyl] -1,3-dimethyl-1 H-purlne-2,6-dlone(1 1)... [Pg.1592]

Draw the structure of Kodel, a polyester prepared by heating dimethyl 1,4-benzenedicarboxylate with l,4-bis(hydroxymethyl)cvclohexane. [Pg.1222]

Ahnliche Eigenschaften wie Lithiumboranat besitzt auch Natrium-trimethoxy-hydri-do-borat1, mit dem z.B. bei 4a,9/ -Dimethyl-8/j-carboxymethyl-4/i,7a-dimcthoxycarbo-nyl-dekalin in 1,2-Dimethoxy-athan bei 85° die sekundare Methoxycarbonyl-Gruppe se-lektiv unter Bildung von 4a,9(i-Dimethyl-7a.-hydroxymethyl-8fi-carboxymethyl-4fi-methoxycarbonyl-dekalin (98°/, d.Th.) reduziert wird2 ... [Pg.201]


See other pages where 1.5- dimethyl-2-hydroxymethyl is mentioned: [Pg.942]    [Pg.35]    [Pg.36]    [Pg.129]    [Pg.129]    [Pg.463]    [Pg.131]    [Pg.365]    [Pg.71]    [Pg.575]    [Pg.1011]    [Pg.1067]    [Pg.1198]    [Pg.1294]    [Pg.1316]    [Pg.1326]    [Pg.349]    [Pg.499]    [Pg.101]    [Pg.91]    [Pg.325]    [Pg.26]    [Pg.148]    [Pg.650]    [Pg.651]    [Pg.668]    [Pg.892]    [Pg.919]    [Pg.251]    [Pg.256]    [Pg.342]    [Pg.1630]    [Pg.910]    [Pg.684]    [Pg.201]   
See also in sourсe #XX -- [ Pg.35 ]




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3.5- Dimethyl-1 -hydroxymethyl-pyrazole

4-hydroxymethyl -2,2-dimethyl -1,3-dioxolane

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