Реакция #40847

ord-8e50eceeef0549698f541ac6041518dd

Уравнение реакции

O=C(Cc1ccccc1)c1ccccc1
deoxybenzoin
CC[O-].[Na+]
NaOEt
CCOC=O
ethyl formate
O=C/C(=C(\O)c1ccccc1)c1ccccc1
title compound
O=C/C(=C(\O)c1ccccc1)c1ccccc1
(Z)-3-Hydroxy-2,3-diphenyl-propenal

Реагенты

Нет

Растворители

Условия реакции

Температура
2.5°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.WAITplaced in the refrigerator for 4 days
  2. 2
    workup.STIRRINGAfter the mixture was stirred overnight at room temperature
  3. 3
    Экстракцияextracted with CH2Cl2
  4. 4
    ПромывкаThe organic layer was washed with brine
  5. 5
    Сушкаdried over MgSO4 anhydride
  6. 6
    Концентрированиеconcentrated in vacuo
  7. 7
    ДругоеThe residue was purified by column chromatography (10% ethyl acetate in hexane)

Методика

To a cooled solution of NaOEt (763 mg, 11.21 mmol) in EtOH (100 ml) was added ethyl formate (0.91 ml, 11.21 mmol) dropwise. The resulting mixture is allowed to stand for 3 hours at 0 to 5° C., and then deoxybenzoin (2 g, 10.19 mmol) was added. The mixture was stirred for 2 hours at 0 to 5° C. and then placed in the refrigerator for 4 days. After the mixture was stirred overnight at room temperature, it was poured into ice-water, and acidified, and extracted with CH2Cl2. The organic layer was washed with brine, and dried over MgSO4 anhydride, and concentrated in vacuo. The residue was purified by column chromatography (10% ethyl acetate in hexane) to give the title compound as a light yellow solid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07728014B2uspto-grants-2010_06