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Hydrochloric Acid → 2-Chloro-4-methyl-5-(4-nitro-phenyl)-thiazole

HRID 908154
ノート
印刷プレビュー

反応式

HRID 908154 の反応式
N(OCCC(C)C)=O.[CH3:9][C:10]1[N:11]=[C:12](N)[S:13][C:14]=1[C:15]1[CH:20]=[CH:19][C:18]([N+:21]([O-:23])=[O:22])=[CH:17][CH:16]=1.[ClH:25]>CC#N.[Cu](Cl)Cl>[Cl:25][C:12]1[S:13][C:14]([C:15]2[CH:20]=[CH:19][C:18]([N+:21]([O-:23])=[O:22])=[CH:17][CH:16]=2)=[C:10]([CH3:9])[N:11]=1
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 3

HCID 313Hydrochloric AcidHCID 8053Isoamyl NitriteHCID 6166034-Methyl-5-(p-nitrophenyl)-2-thiazolamine

生成物 1

HCID 673914002-Chloro-4-methyl-5-(4-nitro-phenyl)-thiazole

試薬・触媒・溶媒 2

HCID 24014Cupric Chloride触媒HCID 6342Acetonitrile溶媒

実験手順

Isoamyl nitrite (3.5 ml, 25 mmol) is added to a stirred suspension/solution of anhydrous copper (II) chloride (2.75 g, 20 mmol) in dry methylcyanide (50 ml). 4-Methyl-5-(4-nitro-phenyl)-thiazol-2-ylamine (25a) (4.0 g, 17 mmol) is then added over 30 minutes. The resulting slurry is stirred at room temperature for 1 hour then heated at 70° C. for 30 minutes. After cooling to room temperature the black solution is poured into 4M hydrochloric acid (200 ml). The product is extracted with ethyl acetate, dried (MgSO4) and the solvent removed to give the title compound as an orange powder (3.13 g). MH+ (TOF, ES+): 255.0

後処理

  1. temperaturethen heated at 70° C. for 30 minutes
  2. temperatureAfter cooling to room temperature the black solution
  3. extractionThe product is extracted with ethyl acetate
  4. dry with materialdried (MgSO4)
  5. customthe solvent removed

出典と根拠

ORDレコード
ord-3e0dd559dc45408d914484da96d8f166
出典データセット
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08017608B2

反応ノート

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