1,3-Benzenedicarboxylic acid, 5-nitro-, 1-methyl ester → 3-Amino-5-(methoxycarbonyl)benzoic acid

HRID 42539

反応式

HRID 42539 の反応式
[CH3:1][O:2][C:3]([C:5]1[CH:6]=[C:7]([CH:11]=[C:12]([N+:14]([O-])=O)[CH:13]=1)[C:8]([OH:10])=[O:9])=[O:4]>CO.[OH-].[OH-].[Pd+2]>[NH2:14][C:12]1[CH:11]=[C:7]([CH:6]=[C:5]([C:3]([O:2][CH3:1])=[O:4])[CH:13]=1)[C:8]([OH:10])=[O:9]

参加物

4

反応物 1

HCID 747761,3-Benzenedicarboxylic acid, 5-nitro-, 1-methyl ester

生成物 1

HCID 135576433-Amino-5-(methoxycarbonyl)benzoic acid収率 92.3%

試薬・触媒・溶媒 2

HCID 9942167Palladium hydroxide触媒HCID 887Methanol溶媒2 回

実験手順

20% Pd(OH)2 (0.50 g) was carefully wetted down under argon with methanol (5 mL) and then 3-(methoxycarbonyl)-5-nitrobenzoic acid (5.00 g, 22.2 mmol) in methanol (20 mL) was added. The mixture was then hydrogenated on a Parr Shaker apparatus for 5 hours at 50 psi. Under argon, the reaction was carefully filtered through a fiberglass filter paper. The filtrate was concentrated to give 3-amino-5-(methoxycarbonyl)benzoic acid (4.0 g, 20.5 mmol, 92% yield) of off-white solids as product. MS found: (M−H)+=194.

後処理

  1. filtrationUnder argon, the reaction was carefully filtered through a fiberglass
  2. filtrationfilter paper
  3. concentrationThe filtrate was concentrated

出典と根拠

ORDレコード
ord-1ee157a6663846bc9fb7d0b8b6770e51
出典データセット
uspto-grants-2013_09
特許番号
US08536198B2

関連ノート

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