2-Benzofurancarboxylic acid, 5-nitro-, ethyl ester → Ethyl 5-aminobenzofuran-2-carboxylate

HRID 1600690

反応式

HRID 1600690 の反応式
[N+:1]([C:4]1[CH:5]=[CH:6][C:7]2[O:11][C:10]([C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:9][C:8]=2[CH:17]=1)([O-])=O>CO.[Ni]>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]2[O:11][C:10]([C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:9][C:8]=2[CH:17]=1

参加物

4

反応物 1

HCID 13829542-Benzofurancarboxylic acid, 5-nitro-, ethyl ester

生成物 1

HCID 9837138Ethyl 5-aminobenzofuran-2-carboxylate

試薬・触媒・溶媒 2

HCID 935Nickel触媒HCID 887Methanol溶媒

実験手順

A solution of 2.3 g of ethyl 5-nitrobenzofuran-2-carboxylate in 60 ml of methanol is hydrogenated in the presence of Raney nickel. The catalyst is filtered off and the solution is concentrated. After customary working up, ethyl 5-aminobenzofuran-2-carboxylate, Rf 0.1 (dichloromethane/ethanol 9.5:0.5) is obtained; hydrochloride m.p. 246-248°.

後処理

  1. filtrationThe catalyst is filtered off
  2. concentrationthe solution is concentrated

出典と根拠

ORDレコード
ord-490c8e3ba36b4061b398ea79c6055a70
出典データセット
uspto-grants-1999_11
特許番号
US05977112

関連ノート

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