تفاعل #631995

ord-b23b071b319f4df2a067183d468ea3a9

معادلة التفاعل

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
المردود 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
المردود 28.4%

المذيبات

ظروف التفاعل

درجة الحرارة
45°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةcooled to room temperature
  2. 2
    غسيلwashed successively with 5% aqueous HCl, 10% aqueous Na2CO3
  3. 3
    تجفيفThe organic phase was dried over Na2SO4
  4. 4
    تركيزconcentrated
  5. 5
    أخرىto afford a brown oil

الإجراء التجريبي

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%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07935669B2uspto-grants-2011_05