ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

4-Phenylcyclohexanone → 4-Phenylcyclohexanol

HRID 1648
ノート
印刷プレビュー

反応式

HRID 1648 の反応式
[C:1]1([CH:7]2[CH2:12][CH2:11][C:10](=[O:13])[CH2:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[BH4-].[Na+]>CO>[C:1]1([CH:7]2[CH2:8][CH2:9][CH:10]([OH:13])[CH2:11][CH2:12]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 786054-PhenylcyclohexanoneHCID 4311764Sodium borohydride

生成物 1

HCID 794974-Phenylcyclohexanol収率 66.2%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 31.4 g (0.18 mol) of 4-phenylcyclohexanone in 500 ml of absolute methanol, which is cooled to -10° C., are added 6.8 g (0.18 mol) of sodium borohydride in batches with stirring. The reaction mixture is allowed to react for 0.5 hours at -10° C. and for 3 hours at ambient temperature and then evaporated down in vacuo. The residue remaining is mixed with water and acidified with 2N hydrochloric acid. The suspension formed is stirred for 1 hour and the crystalline product is suction filtered, dried and recrystallised from diisopropylether. 21 g (66% of theory) of 4-phenylcyclohexanol are obtained, melting point: 112°-114° C.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customto react for 0.5 hours at -10° C. and for 3 hours at ambient temperature
  2. customevaporated down in vacuo
  3. additionThe residue remaining is mixed with water
  4. customThe suspension formed
  5. stirringis stirred for 1 hour
  6. filtrationfiltered
  7. customdried
  8. customrecrystallised from diisopropylether

出典と根拠

ORDレコード
ord-59ad5f10a39944bab640d9fbd6671548
出典データセット
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05726205

反応ノート

読み込み中…