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

Cornforth reagent → 1-[2-Hydroxy-5-(trifluoromethoxy)phenyl]ethan-1-one

HRID 1463279
ノート
印刷プレビュー

反応式

HRID 1463279 の反応式
[F:1][C:2]([F:15])([F:14])[O:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[C:6]([CH:11]([OH:13])[CH3:12])[CH:5]=1.[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=O.[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1>ClCCl>[F:1][C:2]([F:14])([F:15])[O:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[C:6]([C:11](=[O:13])[CH3:12])[CH:5]=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 2724130Cornforth reagentHCID 18987737HCID 18987737、化合物

生成物 1

HCID 27751021-[2-Hydroxy-5-(trifluoromethoxy)phenyl]ethan-1-one収率 85.4%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

In 20 ml of dichloromethane was dissolved 0.85 g (3.83 mmole) of the compound obtained in step 1; and, a suitable amount of Cellite and 1.73 g (4.6 mmole) of pyridinium dichromate were added thereto. The resultant mixture was stirred for 30 minutes at room temperature and filtered by a Cellite layer to obtain precipitates, which were purified by silica gel column chromatography using as an eluent a mixture of hexane and ethyl acetate of 6:1 and then concentrated under reduced pressure at 0° C. to obtain 0.72 g (yield 85%) of the title compound.

後処理

  1. filtrationfiltered by a Cellite layer
  2. customto obtain
  3. customprecipitates
  4. customwhich were purified by silica gel column chromatography
  5. additiona mixture of hexane and ethyl acetate of 6:1
  6. concentrationconcentrated under reduced pressure at 0° C.

出典と根拠

ORDレコード
ord-fb06f018bfc547be9941dd595469b47c
出典データセット
uspto-grants-1994_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05300511

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