반응 #53431

ord-f849e1c730c94e5db84ce2e7ae990baa

반응 방정식

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

용매

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGthe mixture is stirred at 25° C. for 20 h
  2. 2
    농축After concentrating
  3. 3
    기타the residue is partitioned between water and diethyl ether
  4. 4
    건조the ether phase is dried over sodium sulphate
  5. 5
    농축concentrated
  6. 6
    기타The product crystallizes out

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06858622B2uspto-grants-2005_02