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5-Methyl-4-nitro-thiophene-2-carboxylic acid benzyl ester → 5-Methyl-4-amino-thiophene-2-carboxylic acid benzyl ester

HRID 583761
ノート
印刷プレビュー

反応式

HRID 583761 の反応式
[CH2:1]([O:8][C:9]([C:11]1[S:12][C:13]([CH3:19])=[C:14]([N+:16]([O-])=O)[CH:15]=1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>O1CCCC1.[Ni]>[CH2:1]([O:8][C:9]([C:11]1[S:12][C:13]([CH3:19])=[C:14]([NH2:16])[CH:15]=1)=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 381853005-Methyl-4-nitro-thiophene-2-carboxylic acid benzyl ester

生成物 1

HCID 613104205-Methyl-4-amino-thiophene-2-carboxylic acid benzyl ester収率 107%

試薬・触媒・溶媒 2

HCID 935Nickel触媒HCID 8028Tetrahydrofuran溶媒

実験手順

Sponge nickel (0.6 g water wet) was added to a solution of 5-methyl-4-nitro-thiophene-2-carboxylic acid benzyl ester (0.93 g, 3.4 mmol), prepared as described in Step 1 above, in tetrahydrofuran (50 mL), and the mixture was hydrogenated at room temperature under hydrogen atmosphere at a starting pressure of 50 psi. After a reaction time of 2.4 hours, the pressure was released and the mixture filtered. The slurry was rinsed with tetrahydrofuran, and the filtrate was stripped of solvent under reduced pressure, leaving 0.9 g of 5-methyl-4-amino-thiophene-2-carboxylic acid benzyl ester as an oil.

後処理

  1. customprepared
  2. customwas hydrogenated at room temperature under hydrogen atmosphere at a starting pressure of 50 psi
  3. customAfter a reaction time of 2.4 hours
  4. filtrationthe mixture filtered
  5. washThe slurry was rinsed with tetrahydrofuran

出典と根拠

ORDレコード
ord-6daf8a8dedef405e9b97c0fddcb094f5
出典データセット
uspto-grants-2005_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06924276B2

反応ノート

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