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Nitric Acid → 2-Methyl-1-(4-nitrophenyl)propan-2-amine

HRID 1437130
ノート
印刷プレビュー

反応式

HRID 1437130 の反応式
Cl.[CH3:2][C:3]([NH2:12])([CH3:11])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.[N+:13]([O-])([OH:15])=[O:14]>S(=O)(=O)(O)O>[CH3:11][C:3]([NH2:12])([CH3:2])[CH2:4][C:5]1[CH:10]=[CH:9][C:8]([N+:13]([O-:15])=[O:14])=[CH:7][CH:6]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 944Nitric AcidHCID 70969Phentermine Hydrochloride

生成物 1

HCID 138976422-Methyl-1-(4-nitrophenyl)propan-2-amine

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒

反応条件

温度
-10 °C

実験手順

α,α-Dimethylphenethylamine hydrochloride (20 g, 108 mmol) was dissolved in concentrated sulfuric acid (40 mL). The solution was cooled to −10° C. Nitric acid (31 mL, 90%) was added dropwise over a 30 min period while maintaining a reaction temperature below −5° C. The solution was stirred an addition 45 min then poured over ice and allowed to warm to room temperature over night. The product was collected via filtration (13.7 g). Aqueous sodium hydroxide(l N) was added to the filtrate and the title compound was isolated as a clear oil.

後処理

  1. temperaturewhile maintaining a reaction temperature below −5° C
  2. additionan addition 45 min
  3. additionthen poured over ice
  4. temperatureto warm to room temperature over night
  5. filtrationThe product was collected via filtration (13.7 g)
  6. additionAqueous sodium hydroxide(l N) was added to the filtrate

出典と根拠

ORDレコード
ord-b263c502547b45d1b56040fb29f5886d
出典データセット
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07622467B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート