反応 #56499

ord-b9da721fd1b54c3ab4a2f599d27dc867

反応方程式

C=[N+]=[N-]
diazomethane
O=C(O)c1ccc(CCCC2SCC(=O)N2CCC2(O)CCCCC2)cc1
4-{3-[3-[2-(1-hydroxycyclohexyl)ethyl]-4-oxo-2-thiazolidinyl]propyl}benzoic acid
CC(=O)O
Acetic acid
COC(=O)c1ccc(CCCC2SCC(=O)N2CCC2(O)CCCCC2)cc1
title compound
COC(=O)c1ccc(CCCC2SCC(=O)N2CCC2(O)CCCCC2)cc1
Methyl 4-{3-[3-[2-(1-Hydroxycyclohexyl)ethyl]-4-oxo-2-thiazolidinyl]propyl}benzoate

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他to destroy the excess diazomethane
  2. 2
    洗浄the solution is washed with dilute sodium bicarbonate solution
  3. 3
    乾燥dried over sodium sulfate
  4. 4
    その他Evaporation of volatile materials in vacuo

実験手順

A solution of diazomethane (approximately 2.5 g., 0.06 mole) in ether (100 ml.) is mixed with a solution of 4-{3-[3-[2-(1-hydroxycyclohexyl)ethyl]-4-oxo-2-thiazolidinyl]propyl}benzoic acid (11.7 g., 0.03 mole) in ether (100 ml.). The resulting solution is allowed to stand at room temperature for 6 hours. Acetic acid is then added to destroy the excess diazomethane, and the solution is washed with dilute sodium bicarbonate solution and dried over sodium sulfate. Evaporation of volatile materials in vacuo yields the title compound as a nearly colorless, viscous oil.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04225609uspto-grants-1980_09