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

Water → 2-(4-Methylphenyl)cyclohexanone

HRID 458138
ノート
印刷プレビュー

反応式

HRID 458138 の反応式
[C:1]1([CH3:14])[CH:6]=[CH:5][C:4]([CH:7]2[CH2:12][CH2:11][CH2:10][CH2:9][CH:8]2[OH:13])=[CH:3][CH:2]=1.CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.O>ClCCl.COC(C)(C)C>[C:1]1([CH3:14])[CH:2]=[CH:3][C:4]([CH:7]2[CH2:12][CH2:11][CH2:10][CH2:9][C:8]2=[O:13])=[CH:5][CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 962WaterHCID 159087TriacetoxyperiodinaneHCID 27599852-(4-Methylphenyl)cyclohexan-1-ol

生成物 1

HCID 30406522-(4-Methylphenyl)cyclohexanone

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒3 回HCID 15413tert-Butyl methyl ether溶媒

実験手順

To a solution of 3.00 g (15.8 mmol) rac-2-p-tolyl-cyclohexanol in 60 ml dichloromethane were added drop-wise 51.84 g (18.3 mmol) of a 15% solution of Dess-Martin periodinane [1,1,1-tris(acetyloxy)-1,1-dihydro-1,2-benziodoxol-3-(1H)-one] in dichloromethane, and then drop-wise a solution of 300 μl water in 300 ml dichloromethane within 30 min. The resulting solution was stirred for further 30 min. at ambient temperature. Then the reaction mixture was diluted with 350 ml tert.-butyl methyl ether and evaporated to a quarter of the initial volume. The residue was diluted with 800 ml tert.-butyl methyl ether, washed with a total of 600 ml of a 1:1 mixture of saturated NaHCO3 solution and a 10% Na2S2O3 solution and with brine. The combined aqueous extracts were re-extracted with tert.-butyl methyl ether. The combined organic extracts were washed with brine, died over Na2SO4, filtered and evaporated. The residue was purified by flash-chromatography on silica gel with dichloromethane as eluent: 2.39 g rac-2-p-tolyl-cydohexanone as colorless powder: MS (ISP): 189.3 MH+.

後処理

  1. customwithin 30 min
  2. customevaporated to a quarter of the initial volume
  3. additionThe residue was diluted with 800 ml tert.-butyl methyl ether
  4. washwashed with a total of 600 ml of a 1:1 mixture of saturated NaHCO3 solution
  5. extractionThe combined aqueous extracts were re-extracted with tert.-butyl methyl ether
  6. washThe combined organic extracts were washed with brine
  7. filtrationfiltered
  8. customevaporated
  9. customThe residue was purified by flash-chromatography on silica gel with dichloromethane as eluent

出典と根拠

ORDレコード
ord-ca1ca33ea8e642e6bdc1bdcc3f485955
出典データセット
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07189850B2

反応ノート

読み込み中…

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