Dichloromethane → n,n-Dimethyl-2-(4-nitrophenyl)ethanamine

HRID 1670798

反応式

HRID 1670798 の反応式
Cl.[CH3:2][NH:3][CH3:4].[N+:5]([C:8]1[CH:16]=[CH:15][C:11]([CH2:12][CH2:13]Br)=[CH:10][CH:9]=1)([O-:7])=[O:6].C(N(CC)C(C)C)(C)C.ClCCl>CN(C)C=O.O>[CH3:2][N:3]([CH3:4])[CH2:13][CH2:12][C:11]1[CH:15]=[CH:16][C:8]([N+:5]([O-:7])=[O:6])=[CH:9][CH:10]=1

参加物

7

反応条件

温度
60 °C

実験手順

Dimethylamine hydrochloride (0.390 g, 4.78 mmol) was added to a solution containing 4-nitrophenethyl bromide (1.0 g, 4.35 mmol) and N, N-diisopropylethyamine (1.69 g, 13.05 mmol) in anhydrous dimethylformamide (20 mL). The reaction mixture was heated to 60° C. for 5 hours, then allowed to cool. The solution was diluted with 1:1 water:dichloromethane (200 mL), then added to a separatory funnel. The organics were collected and the product was extracted with 1N aqueous hydrogen chloride. The organics were removed and the aqueous layer was made basic with 1N aqueous sodium hydroxide. The product was extracted with dichloromethane (100 mL) and washed with saturated aqueous sodium chloride (200 mL). The organics were dried over magnesium sulfate and the solvent removed at reduced pressure to afford the title intermediate (0.426 g crude) as a clear oil, which was used without further purification.

後処理

  1. temperatureto cool
  2. customThe organics were collected
  3. extractionthe product was extracted with 1N aqueous hydrogen chloride
  4. customThe organics were removed
  5. extractionThe product was extracted with dichloromethane (100 mL)
  6. washwashed with saturated aqueous sodium chloride (200 mL)
  7. dry with materialThe organics were dried over magnesium sulfate
  8. customthe solvent removed at reduced pressure

出典と根拠

ORDレコード
ord-aeddd6dbd94b4792aa6c984e487fbde1
出典データセット
uspto-grants-2011_08
特許番号
US07994165B2

関連ノート

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