1-Chlorobutane-2,3-dione → 1-(2-Amino-1,3-thiazol-4-yl)ethan-1-one

HRID 2222989ノート

反応式

HRID 2222989 の反応式
[NH2:1][C:2]([NH2:4])=[S:3].Cl[CH2:6][C:7](=O)[C:8](=[O:10])[CH3:9]>C(O)C>[NH2:1][C:2]1[S:3][CH:6]=[C:7]([C:8](=[O:10])[CH3:9])[N:4]=1

参加物

4

実験手順

To a solution of thiourea (6.79 g, 89.2 mmol) in absolute ethanol (100 mL) was added 1-chloro-butane-2,3-dione (prepared as described by Bonnema, J. et al., Rec. Trav. Chim. Pays-Bas 1960, 79, 1137) (10.75 g, 89.2 mmol) and the mixture stirred at room temperature for 72 hours. The dark brown suspension was concentrated in vacuo, the residue taken up in water (350 mL), acidified with 1M aqueous hydrochloric acid (20 mL) and extracted with ethyl acetate (2×100 mL). The aqueous layer was then neutralized with solid sodium bicarbonate to form a light brown solid which was isolated by filtration. The precipitate was washed with 1:1 hexanes/ether (100 mL), 1:1 hexanes/ethyl acetae (100 mL) and then dried in vacuo over potassium hydroxide to give 1-(2-amino-thiazol-4-yl)-ethanone as a light brown solid (9.91 g, 78%).

後処理

  1. concentrationThe dark brown suspension was concentrated in vacuo
  2. extractionextracted with ethyl acetate (2×100 mL)
  3. customto form a light brown solid which
  4. customwas isolated by filtration
  5. washThe precipitate was washed with 1:1 hexanes/ether (100 mL), 1:1 hexanes/ethyl acetae (100 mL)
  6. dry with materialdried in vacuo over potassium hydroxide

出典と根拠

ORDレコード
ord-d0d76255766a46cb94c887d21477f974
出典データセット
uspto-grants-2008_05
特許番号
US07371869B2

反応ノート

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