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Methanol → Methyl 3-amino-4-propylbenzoate

HRID 1072879
ノート
印刷プレビュー

反応式

HRID 1072879 の反応式
[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][C:12]=1[CH2:13][CH2:14][CH3:15])[C:7]([OH:9])=[O:8])([O-])=O.S(=O)(=O)(O)O.[CH3:21]O>[Pd]>[NH2:1][C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][C:12]=1[CH2:13][CH2:14][CH3:15])[C:7]([O:9][CH3:21])=[O:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 155216373-Nitro-4-propylbenzoic acid

生成物 1

HCID 22387873Methyl 3-amino-4-propylbenzoate

試薬・触媒・溶媒 1

HCID 23938Palladium触媒

実験手順

To 3-nitro-4-propylbenzoic acid (31.0 g) were added sulfuric acid (1.0 g) and methanol (300 ml) and the mixture was heated under reflux for 24 hr. After cooling, 5% Pd-C (0.60 g) was added to the reaction mixture and the mixture was stirred under a hydrogen atmosphere (normal pressure) for 6 hr. The reaction mixture was filtered through Celite and concentrated. To the residue was added a saturated aqueous sodium hydrogencarbonate solution, and the mixture was extracted with toluene. The toluene layer was dried over sodium sulfate and concentrated to give the object compound (28.7 g) as an brown oil.

後処理

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 24 hr
  3. temperatureAfter cooling
  4. filtrationThe reaction mixture was filtered through Celite
  5. concentrationconcentrated
  6. additionTo the residue was added a saturated aqueous sodium hydrogencarbonate solution
  7. extractionthe mixture was extracted with toluene
  8. dry with materialThe toluene layer was dried over sodium sulfate
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-b963fd9283674be3926408622d4e3b94
出典データセット
uspto-grants-2005_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06911469B2

反応ノート

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