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Methanol → Methyl 4-chloro-3-mercapto-2-methylbenzoate

HRID 548590
ノート
印刷プレビュー

反応式

HRID 548590 の反応式
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([CH3:11])[C:3]=1[SH:12].[CH3:13]O>S(=O)(=O)(O)O.O>[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([O:8][CH3:13])=[O:7])=[C:4]([CH3:11])[C:3]=1[SH:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 887MethanolHCID 667391434-Chloro-3-mercapto-2-methylbenzoic acid

生成物 1

HCID 67158973Methyl 4-chloro-3-mercapto-2-methylbenzoate

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 1118Sulfuric Acid溶媒

実験手順

Under an atmosphere of nitrogen, 3.60 g (17.8 mmol) of 4-chloro-3-mercapto-2-methylbenzoic acid in 50 ml of absolute methanol and 1 ml of concentrated sulfuric acid were heated under reflux for 17 h. The mixture was freed from solvent, and the residue was taken up in water. After two extractions with ethyl acetate, the combined organic phases were dried, filtered under an atmosphere of nitrogen and freed from the solvent. What was isolated were 3.2 g of pure product.

後処理

  1. temperatureunder reflux for 17 h
  2. extractionAfter two extractions with ethyl acetate
  3. customthe combined organic phases were dried
  4. filtrationfiltered under an atmosphere of nitrogen
  5. customWhat was isolated

出典と根拠

ORDレコード
ord-6d856e14df4a4ee1968b35f8c1ac6b7c
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07943551B2

反応ノート

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