反应 #53431

ord-f849e1c730c94e5db84ce2e7ae990baa

反应方程式

BrC1CCCC1
cyclopentyl bromide
CC(C)(C)[O-].[K+]
potassium tert-butoxide
Cc1ccc(CC(=O)OC(C)(C)C)cc1
compound
Cc1ccc(CC(=O)OC(C)(C)C)cc1
tert-Butyl 4-methylphenyl-acetate
Cc1ccc(C(C(=O)OC(C)(C)C)C2CCCC2)cc1
tert-Butyl 2-Cyclopentyl-2-(4-methylphenyl)acetate

溶剂

反应条件

温度
0°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGthe mixture is stirred at 25° C. for 20 h
  2. 2
    浓缩After concentrating
  3. 3
    其他the residue is partitioned between water and diethyl ether
  4. 4
    干燥the ether phase is dried over sodium sulphate
  5. 5
    浓缩concentrated
  6. 6
    其他The product crystallizes out

实验过程

33.5 g, (0.3 mol of potassium tert-butoxide are initially introduced into 100 ml of anhydrous DMF at 0° C., and 51.6 g (0.25 mol) of the compound from Example XX in 250 ml of anhydrous DMF are added dropwise. The mixture is stirred at 0° C. for 30 min and 32.2 ml (0.3 mol) of cyclopentyl bromide in 150 ml of anhydrous DMF are added dropwise at 5-15° C. and the mixture is stirred at 25° C. for 20 h. After concentrating, the residue is partitioned between water and diethyl ether, and the ether phase is dried over sodium sulphate and concentrated. The product crystallizes out.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06858622B2uspto-grants-2005_02