反応 #631995

ord-b23b071b319f4df2a067183d468ea3a9

反応方程式

O=C(Cl)c1ccccc1
Benzoyl chloride
C=CCCC(=O)C1CC(C)(C)CCC1O
1-(2-hydroxy-5,5-dimethyl-1-cyclohexyl)-4-penten-1-one
CCN(CC)CC
Et3N
C1CCCCC1.CCOC(C)=O
AcOEt Cyclohexane
C=CCCC(=O)[C@H]1CC(C)(C)CC[C@H]1OC(=O)c1ccccc1
title compound
収率 28.4%
C=CCCC(=O)[C@H]1CC(C)(C)CC[C@H]1OC(=O)c1ccccc1
cis-4,4-dimethyl-2-(4-pentenoyl)cyclohexyl Benzoate
収率 28.4%

溶媒

反応条件

温度
45°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度cooled to room temperature
  2. 2
    洗浄washed successively with 5% aqueous HCl, 10% aqueous Na2CO3
  3. 3
    乾燥The organic phase was dried over Na2SO4
  4. 4
    濃縮concentrated
  5. 5
    その他to afford a brown oil

実験手順

Benzoyl chloride (12.8 g, 91 mmoles) was added dropwise to a stirred solution of 1-(2-hydroxy-5,5-dimethyl-1-cyclohexyl)-4-penten-1-one (16 g, 75 mmoles), Et3N (10 g, 99 mmoles) and DMAP (1.8 g, 15 mmoles) in CH2Cl2 (380 ml) at 20° C. and under nitrogen. The solution was heated at 45° C. during 22 hours, cooled to room temperature and washed successively with 5% aqueous HCl, 10% aqueous Na2CO3, and again with water. The organic phase was dried over Na2SO4 and concentrated to afford a brown oil. Chromatography (SiO2, AcOEt/Cyclohexane 1:9) and afforded 6.7 g of the title compound (yield=28%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07935669B2uspto-grants-2011_05