Methyl 7-nitrobenzo[b]thiophene-2-carboxylate → Methyl 7-amino-1-benzothiophene-2-carboxylate
反応式
[CH3:1][O:2][C:3]([C:5]1[S:9][C:8]2[C:10]([N+:14]([O-])=O)=[CH:11][CH:12]=[CH:13][C:7]=2[CH:6]=1)=[O:4]>C(O)(=O)C.Cl>[CH3:1][O:2][C:3]([C:5]1[S:9][C:8]2[C:10]([NH2:14])=[CH:11][CH:12]=[CH:13][C:7]=2[CH:6]=1)=[O:4]参加物
実験手順
To a mixture of 7-nitro-benzo[b]thiophene-2-carboxylic acid methyl ester (100 mg) in acetic acid (4 mL) was added a solution of SnC2.2H2O (10 eq) in 1.5 mL of concentrated HCl. The reaction was stirred at room temperature 12 h. The excess acid was partially removed in vacuo, and the reaction mixture was then poured into a flask (250 mL) and was neutralized with saturated NaHCO3 solution at 0° C. The pH was brought up to pH 9 by adding solid NaHCO3. The resulting aqueous mixture was diluted with EtOAc, and the Tin-by product was removed by filtering through a pad of diatomaceous earth. The pad was rinsed with EtOAc and the combined filtrates were partitioned in a separatory funnel. The aqueous layer was extracted with EtOAc two times times. The combined organics were dried over MgSO4, filtered and concentrated to give the desired 7-amino-benzo[b]thiophene-2-carboxylic acid methyl ester (100%).
後処理
- customThe excess acid was partially removed in vacuo
- additionthe reaction mixture was then poured into a flask (250 mL)
- customwas neutralized with saturated NaHCO3 solution at 0° C
- additionby adding solid NaHCO3
- additionThe resulting aqueous mixture was diluted with EtOAc
- customthe Tin-by product was removed
- filtrationby filtering through a pad of diatomaceous earth
- washThe pad was rinsed with EtOAc
- customthe combined filtrates were partitioned in a separatory funnel
- extractionThe aqueous layer was extracted with EtOAc two times times
- dry with materialThe combined organics were dried over MgSO4
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-3be63abe472f44f9b1eb7d94f1922fc9
- 出典データセット
- uspto-grants-2009_06
- 特許番号
- US07550461B2
反応ノート
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