p-Toluenesulfonic acid → 1-Hydroxy-2-cyclopentyltetraline

HRID 597104

反応式

HRID 597104 の反応式
[CH:1]1[CH2:5][CH2:4][CH2:3][CH:2]=1.[OH:6][CH:7]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH2:10][CH2:9][CH2:8]1.C1(C)C=CC(S(O)(=O)=O)=CC=1>>[OH:6][CH:7]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH2:10][CH2:9][CH:8]1[CH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1

参加物

4

反応物 3

HCID 6101p-Toluenesulfonic acidHCID 8882CyclopenteneHCID 107231,2,3,4-Tetrahydro-1-naphthalenol

生成物 1

HCID 214465011-Hydroxy-2-cyclopentyltetraline

実験手順

40 g of cyclopentene are added dropwise at 120° C to 148 g of 1-hydroxytetraline and 10 g of p-toluene sulphonic acid. The catalyst is removed by washing with sodium hydrogen carbonate solution. The reaction mixture is fractionated. At 161° C (2 mm Hg) 58 g of 1-hydroxy-2-cyclopentyltetraline are obtained.

後処理

  1. customThe catalyst is removed
  2. washby washing with sodium hydrogen carbonate solution

出典と根拠

ORDレコード
ord-70f6c25426584fe8b20a2d854275c8fa
出典データセット
uspto-grants-1977_03
特許番号
US04013473

関連ノート

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