反应 #1909789

ord-26b0044b4c1447408ddcf5b03a53b74a

反应方程式

[H][H]
hydrogen
COC(=O)c1ccc(C=CCCNCC(=O)OC(C)(C)C)cc1O
( 1 )
COC(=O)c1ccc(C=CCCNCC(=O)OC(C)(C)C)cc1O
4-[4-(tert-Butoxycarbonylmethylamino)-1-butenyl]-2-hydroxybenzoic acid methyl ester
COC(=O)c1ccc(CCCCNCC(=O)OC(C)(C)C)cc1O
title compound
收率 95.0%
COC(=O)c1ccc(CCCCNCC(=O)OC(C)(C)C)cc1O
4-[4-(tert-Butoxycarbonylmethylamino)butyl]-2-hydroxybenzoic acid methyl ester
收率 95.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤After filtering through Celite
  2. 2
    浓缩the mixture was concentrated under reduced pressure
  3. 3
    其他the residue was purified by silica gel column chromatography (developing solvent: hexane/ethyl acetate=4/1 v/v)

实验过程

A solution of the compound (0.845 g) obtained in (1) above in methanol (20 ml) was vigorously stirred in the presence of 10% palladium-carbon (0.106 g) in a stream of hydrogen. After filtering through Celite, the mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (developing solvent: hexane/ethyl acetate=4/1 v/v) to give the title compound (0.810 g, yield 95%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE039088E1uspto-grants-2006_05