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Methanethiol → 4-Chloro-3-(methylsulphenyl)-2-(methylsulphonyl)benzoic acid

HRID 341733
ノート
印刷プレビュー

反応式

HRID 341733 の反応式
O.[OH-].[Li+].[CH3:4][SH:5].[Cl:6][C:7]1[CH:15]=[CH:14][C:10]([C:11]([OH:13])=[O:12])=[C:9]([S:16]([CH3:19])(=[O:18])=[O:17])[C:8]=1F.O>CN(C)C=O>[Cl:6][C:7]1[CH:15]=[CH:14][C:10]([C:11]([OH:13])=[O:12])=[C:9]([S:16]([CH3:19])(=[O:18])=[O:17])[C:8]=1[S:5][CH3:4]
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 4

HCID 878MethanethiolHCID 962WaterHCID 168937Lithium hydroxide, monohydrateHCID 544424304-Chloro-3-fluoro-2-methylsulphonylbenzoic acid

生成物 1

HCID 536334514-Chloro-3-(methylsulphenyl)-2-(methylsulphonyl)benzoic acid収率 55%

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒

実験手順

Lithium hydroxide monohydrate (1.26 g) was added to a solution of methyl mercaptan (0.72 g) in dimethyl formamide. To this mixture was added 4-chloro-3-fluoro-2-(methylsulphonyl)benzoic acid (3.7 g). The mixture was stirred for 2 hours then poured into water and acidified to pH1. It was extracted with ether, washed with water, dried (Na2SO4) and filtered. The filtrate was evaporated to dryness and the residue was triturated with n-hexane and filtered to give 4-chloro-3-(methylsulphenyl)-2-(methylsulphonyl)benzoic acid (2.26 g) as a white solid, NMR (CDCl3) 2.5(s,3H), 3.45(s,3H), 7.5(d,1H), 7.7(d,1H).

後処理

  1. extractionIt was extracted with ether
  2. washwashed with water
  3. dry with materialdried (Na2SO4)
  4. filtrationfiltered
  5. customThe filtrate was evaporated to dryness
  6. customthe residue was triturated with n-hexane
  7. filtrationfiltered

出典と根拠

ORDレコード
ord-4eb30192f8e248068641c6975323a920
出典データセット
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05856274

反応ノート

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