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Ethanol → 3-Thiazol-4-yl-benzoic acid methyl ester

HRID 1265611
ノート
印刷プレビュー

反応式

HRID 1265611 の反応式
Br[CH2:2][C:3]([C:5]1[CH:6]=[C:7]([CH:11]=[CH:12][CH:13]=1)[C:8]([OH:10])=[O:9])=O.[CH:14]([NH2:16])=[S:15].[CH3:17]CO>>[CH3:17][O:10][C:8](=[O:9])[C:7]1[CH:11]=[CH:12][CH:13]=[C:5]([C:3]2[N:16]=[CH:14][S:15][CH:2]=2)[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

4

反応物 3

HCID 702EthanolHCID 27568353-(Bromoacetyl)benzoic acidHCID 3005587Methanethioamide

生成物 1

HCID 696880593-Thiazol-4-yl-benzoic acid methyl ester

実験手順

A solution of 3-(2-bromo-acetyl)-benzoic acid (1.22 g) and thioformamide (0.46 g) in EtOH (5 mL) was heated to 80° C. for 1 h. The mixture was partitioned between AcOEt and brine and the organic layer was dried and evaporated. The residual oil was dissolved in a mixture of MeOH (20 mL) and 4NHCl/Et2O (5 mL). After being kept at 20° C. for 18 h, the solution was concentrated in vacuum, diluted with AcOEt, washed with sat. NaHCO3 solution and brine, dried and evaporated. The residue was chromatographed on silica gel using AcOEt/hexane (1:3) as eluent to give 3-thiazol-4-yl-benzoic acid methyl ester (0.98 g) as off-white solid, MS (ISP) 220.2 [(M+H)+].

後処理

  1. customThe mixture was partitioned between AcOEt and brine
  2. customthe organic layer was dried
  3. customevaporated
  4. dissolutionThe residual oil was dissolved in a mixture of MeOH (20 mL)
  5. concentrationthe solution was concentrated in vacuum
  6. additiondiluted with AcOEt
  7. washwashed with sat. NaHCO3 solution and brine
  8. customdried
  9. customevaporated
  10. customThe residue was chromatographed on silica gel

出典と根拠

ORDレコード
ord-0e5bb50fdc0a4472908fd6afad97d366
出典データセット
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06544985B2

反応ノート

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