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Hydrazine hydrate (1:1) → 3-(1,3-Thiazol-2-yl)aniline

HRID 2262749
ノート
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反応式

HRID 2262749 の反応式
Cl[C:2]1[S:6][C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[C:9]([N+:13]([O-])=O)[CH:8]=2)=[N:4][CH:3]=1.O.NN>C1COCC1.[Ni]>[S:6]1[CH:2]=[CH:3][N:4]=[C:5]1[C:7]1[CH:8]=[C:9]([NH2:13])[CH:10]=[CH:11][CH:12]=1
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 24654Hydrazine hydrate (1:1)HCID 575722385-Chloro-2-(3-nitro-phenyl)-thiazole

生成物 1

HCID 110193903-(1,3-Thiazol-2-yl)aniline収率 86.4%

試薬・触媒・溶媒 2

HCID 935Nickel触媒HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 5-chloro-2-(3-nitro-phenyl)-thiazole (20.0 g, 69.6 mmol) in THF (260 ml) was added hydrazine monohydrate (13.5 ml, 278 mmol) and Raney nickel (2 g). The resultant mixture was stirred at ambient conditions for 1 hour and then filtered through celite. The filtrate was evaporated to dryness and the filtrate was partitioned between ethyl acetate and saturated, aqueous sodium carbonate. The organic layer was dried over sodium sulphate and concentrated in vacuo. The concentrate was eluted through silica gel with a mixture of ethyl acetate and ligroin (1:3 v/v) to afford the desired product (10.6 g, 72%).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. filtrationfiltered through celite
  2. customThe filtrate was evaporated to dryness
  3. customthe filtrate was partitioned between ethyl acetate
  4. dry with materialThe organic layer was dried over sodium sulphate
  5. concentrationconcentrated in vacuo
  6. washThe concentrate was eluted through silica gel with a mixture of ethyl acetate and ligroin (1:3 v/v)

出典と根拠

ORDレコード
ord-245ad76fcb924d85a64583802b27a633
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07851490B2

反応ノート

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