反応 #9360

ord-37e41d6c8bde4a8c90ee4691de966a73

反応方程式

COC(=O)C#N
Methyl cyanoformate
CN(C)P(=O)(N(C)C)N(C)C
HMPA
CC(C)[N-]C(C)C.[Li+]
LDA
O=C1CCC(CCOCc2ccccc2)CC1
4-(2-benzyloxy-ethyl)-cyclohexanone
COC(=O)C1CCCCC1
cyclohexanecarboxylic acid methyl ester

溶媒

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度before re-cooling to −78° C.
  2. 2
    その他before aqueous quench
  3. 3
    その他The product was purified by chromatography on SiO2 with 10% EtOAc

実験手順

A solution of LDA (33 ml, 1.5 M in Et2O) in THF (50 mL) at −78° C. was treated with 4-(2-benzyloxy-ethyl)-cyclohexanone (9.5 g, 40.2 mmol). The mixture was warmed to 0° C. over 30 min. before re-cooling to −78° C. and adding HMPA (7 mL). Methyl cyanoformate (CNCO2Me, 4.1 mL, 85 mmol) was added and the mixture was stirred for 15 m before aqueous quench and work-up. The product was purified by chromatography on SiO2 with 10% EtOAc:Hx. 5-(2-Benzyloxy-ethyl)-2-oxo-)cyclohexanecarboxylic acid methyl ester was isolated, 5.8 g (49%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07091232B2uspto-grants-2006_08