Dimethylformamide dimethyl acetal → 4-(4-Chlorophenoxy)-1-(dimethylamino)pent-1-en-3-one

HRID 1290796

반응식

HRID 1290796 반응식
[Cl:1][C:2]1[CH:13]=[CH:12][C:5]([O:6][CH:7]([CH3:11])[C:8](=[O:10])[CH3:9])=[CH:4][CH:3]=1.CO[CH:16](OC)[N:17]([CH3:19])[CH3:18]>CO>[Cl:1][C:2]1[CH:13]=[CH:12][C:5]([O:6][CH:7]([CH3:11])[C:8](=[O:10])[CH:9]=[CH:16][N:17]([CH3:19])[CH3:18])=[CH:4][CH:3]=1

참가 물질

4

반응물 2

HCID 78373Dimethylformamide dimethyl acetalHCID 37226323-(4-Chlorophenoxy)-2-butanone

생성물 1

HCID 37226344-(4-Chlorophenoxy)-1-(dimethylamino)pent-1-en-3-one

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
120 °C

실험 절차

A mixture of 3-(4-chlorophenoxy)-2-butanone (34.50 g) and N,N-dimethylformamide dimethylacetal (20.70 g) was heated under argon in an oil bath at 120° C. for 13 hours. The methanol produced in the reaction was removed under reduced pressure and the residual oil triturated with n-hexane. The solid was collected by filtration and washed with cold diethyl ether to give 4-(4-chlorophenoxy)-1-(dimethylamino)-1-penten-3-one. Yield 32.50 g.

후처리

  1. customwas removed under reduced pressure
  2. customthe residual oil triturated with n-hexane
  3. filtrationThe solid was collected by filtration
  4. washwashed with cold diethyl ether

출처 및 근거

ORD 기록
ord-668f3b7f3407401e8cf080dfc7ea133b
출처 데이터셋
uspto-grants-1998_05
특허 번호
US05753665

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