Реакция #1797476

ord-794c8f297053424c8fe452c51e7a9bea

Уравнение реакции

[O]=[Cr](=[O])([O-])[Cl].c1cc[nH+]cc1
PCC
CCCCCCCCC(CCCCCO)OCc1ccccc1
6-benzyloxy-1-tetradecanol
CCCCCCCCC(CCCCC=O)OCc1ccccc1
6-benzyloxy-tetradecanal

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Фильтрацияfiltered through a bed of silica gel

Методика

PCC (9.7 g, 45 mmol) was added in portions to a solution containing 6-benzyloxy-1-tetradecanol (7.5 g, 30 mmol) in methylene chloride (100 ml) at RT. The black mixture was stirred for 2 hours, then filtered through a bed of silica gel using hexane:ethyl acetate (90:10). The corresponding aldehyde, 6-benzyloxy-tetradecanal, was produced at a yield of 6.1 g (81%). This aldehyde compound was mixed with carbethoxymethylene triphenylphosphorane (10 g, 29 mmol) in 100 ml of methylene chloride at RT. The mixture was allowed to stir overnight, after which the solvent was removed and replaced with hexane. Solid precipitates were removed by filtration. Following chromatography on silica gel using hexane:ethyl acetate at a ratio of 90:10, the corresponding ester was detected at 8.4 g scale (90%). The chemical shift of the ester, 8-benzyloxyhexadec-2-enoate ethyl ester, is as follows: 1H-NMR (CDCl3) δ 0.89 (m, 6H, CH3), 1.2-1.5 (m, 20H, CH2), 2.2 (m, 2H, CH2—C═), 3.35 (m, 2H, CH2O), 4.2 (q, 2H, MeCH2—O), 4.55 (dd, 2H, CH2—O), 5.8 (d, 1H, CH═C), 6.95 (d,t 1H, CH═C), 7.35 (m, 5H, benzyl).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07790142B2uspto-grants-2010_09