반응 #320288

ord-139b224165174673a406045bcf5d1011

반응 방정식

CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(C)(C)CCC3=O)cc1
ethyl 4-[(5,6,7,8-tetrahydro-8,8-dimethyl-5-oxonaphth-2-yl)ethynyl]benzoate
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(C)(C)CCC3=O)cc1
Compound 1
CCOC(=O)c1ccc(C#Cc2ccc3c(c2)C(C)(C)CCC3=O)cc1
ethyl 4-[(5,6,7,8-tetrahydro-8,8-dimethyl-5-oxonaphth-2-yl)ethynyl]benzoate
[Li+].[OH-]
LiOH
CC1(C)CCC(=O)c2ccc(C#Cc3ccc(C(=O)O)cc3)cc21
title compound
CC1(C)CCC(=O)c2ccc(C#Cc3ccc(C(=O)O)cc3)cc21
4-[(5,6,7,8-tetrahydro-8,8-dimethyl-5-oxonaphth-2-yl)ethynyl]benzoic acid

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축concentrated in vacuo
  2. 2
    기타partitioned between EtOAc and 1 ml of water
  3. 3
    추출The aqueous layer was extracted with EtOAc
  4. 4
    건조the organic layer was dried over Na2SO4
  5. 5
    농축concentrated in vacuo

실험 절차

To a suspension of 0.30 g (0.87 mmol) of ethyl 4-[(5,6,7,8-tetrahydro-8,8-dimethyl-5-oxonaphth-2-yl)ethynyl]benzoate (Compound 1) in 4 ml of THF and 2 ml of ethanol was added 2 ml (2 mmol) of LiOH (1N aqueous solution). The reaction mixture was stirred at room temperature for 4 hours, concentrated in vacuo to near dryness, partitioned between EtOAc and 1 ml of water and acidified to pH 4 with 10% HCl. The aqueous layer was extracted with EtOAc and then the organic layer was dried over Na2SO4 and concentrated in vacuo to give the title compound as a light yellow solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05591858uspto-grants-1997_01