1-Fluoro-4-methanesulfonyl-2-nitrobenzene → 2-Fluoro-5-(methylsulfonyl)aniline

HRID 2390165

反応式

HRID 2390165 の反応式
[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][C:8]([F:11])=[C:7]([N+:12]([O-])=O)[CH:6]=1)(=[O:4])=[O:3].[H][H]>CO.O=[Pt]=O>[F:11][C:8]1[CH:9]=[CH:10][C:5]([S:2]([CH3:1])(=[O:4])=[O:3])=[CH:6][C:7]=1[NH2:12]

参加物

5

反応物 2

HCID 3131371-Fluoro-4-methanesulfonyl-2-nitrobenzeneHCID 178418361HCID 178418361、化合物

生成物 1

HCID 27746372-Fluoro-5-(methylsulfonyl)aniline収率 111.7%

試薬・触媒・溶媒 2

HCID 345198Adams' catalyst触媒HCID 887Methanol溶媒

実験手順

A mixture of 4-fluoro-3-nitrophenyl methyl sulfone (Acros; 1.00 g; 4.56 mmol) and PtO2 (100 mg) in MeOH (150 ml) was placed in a PARR reactor and treated with a pressure of 20 atm of hydrogen for 3 hours. The reaction mixture was filtered through Celite and the filtrate was concentrated to dryness affording the title compound (964 mg) as a dark green oil.

後処理

  1. customwas placed in a PARR reactor
  2. filtrationThe reaction mixture was filtered through Celite
  3. concentrationthe filtrate was concentrated to dryness

出典と根拠

ORDレコード
ord-f86a52444a864fd7bb82a00530047304
出典データセット
uspto-grants-2012_09
特許番号
US08273769B2

関連ノート

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