反応 #1482

ord-71d8a412e47743ae868fcc2cf8c525e8

反応方程式

OCCO
ethylene glycol
CC(=O)c1ccc2c(c1)C(=O)CCC2(C)C
3,4-dihydro-4,4-dimethyl-7-acetyl-naphthalen-1(2H)-one
Cc1ccc(S(=O)(=O)O)cc1.O
p-toluenesulfonic acid monohydrate
CC(=O)c1ccc2c(c1)C(C)(C)CCC2=O
3,4-dihydro-4,4-dimethyl-6-acetyl-naphthalen-1(2H)-one
CC1(C)CCC(=O)c2ccc(C3(C)OCCO3)cc21
title compound
CC1(C)CCC(=O)c2ccc(C3(C)OCCO3)cc21
6-(2-methyl-1,3-dioxolan-2-yl)-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The resulting solution was heated
  2. 2
    温度to reflux for 18 h
  3. 3
    濃縮concentrated under reduced pressure

実験手順

A solution of 1.80 g (8.34 mmol) of a 1:5 mixture of 3,4-dihydro-4,4-dimethyl-7-acetyl-naphthalen-1(2H)-one (Compound D14a); and 3,4-dihydro-4,4-dimethyl-6-acetyl-naphthalen-1(2H)-one (Compound D14b) in 50 mL benzene was combined with 517.7 mg (8.34 mmol) of ethylene glycol and 20.0 mg (0.11 mmol) of p-toluenesulfonic acid monohydrate. The resulting solution was heated to reflux for 18 h, cooled to room temperature, and concentrated under reduced pressure. The title compound was isolated by column chromatography (10% EtOAc-hexanes) as a colorless oil.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05723666uspto-grants-1998_03