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

HRID 1670798

반응식

HRID 1670798 반응식
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

참가 물질

7

반응 조건

온도
60 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-aeddd6dbd94b4792aa6c984e487fbde1
출처 데이터셋
uspto-grants-2011_08
특허 번호
US07994165B2

연결된 노트

불러오는 중…