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Propanamide, N,N-dimethyl- → 1-(2,2-Difluoro-1,3-benzodioxol-4-yl)propanone

HRID 1376320
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인쇄 미리보기

반응식

HRID 1376320 반응식
CN(C)[C:3](=[O:6])[CH2:4]C.[F:8][C:9]1([F:18])[O:13][C:12]2[CH:14]=[CH:15][CH:16]=[CH:17][C:11]=2[O:10]1.[CH3:19]OC(OC)N(C)C>>[F:18][C:9]1([F:8])[O:10][C:11]2[CH:17]=[CH:16][CH:15]=[C:14]([CH2:19][C:3](=[O:6])[CH3:4])[C:12]=2[O:13]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 12965Propanamide, N,N-dimethyl-HCID 741032,2-Difluoro-1,3-benzodioxoleHCID 78373Dimethylformamide dimethyl acetal

생성물 1

HCID 229164921-(2,2-Difluoro-1,3-benzodioxol-4-yl)propanone

반응 조건

온도
70 °C

실험 절차

12 g of 1-(2,2-difluoro-1,3-benzodioxol-4-yl)propanone are prepared by condensation-of N,N-dimethylpropionamide with the lithiated anion of 2,2-difluoro-1,3-benzodioxole obtained according to the procedure described in patent EP 333658, are then dissolved in 14.6 ml (0.11 mol) of N,N-dimethylformamide dimethyl acetal and heated at 70° C. according to the procedure described in Example No. 1. 25 g (0.05 mol) of enaminone thus obtained are dissolved in 130 ml of acetic acid and then 3.3 ml (0.069 mol) of hydrazine hydrate are added. The crude product obtained is purified by trituration in pentane.

후처리

  1. customobtained

출처 및 근거

ORD 기록
ord-16a5dc7e4c0e43639dba07e459f81a7b
출처 데이터셋
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05663119

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