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Allyl bromide → HCID 20566762, 화합물

HRID 847671
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HRID 847671 반응식
[CH2:1]([NH:5][S:6]([C:9]([F:12])([F:11])[F:10])(=[O:8])=[O:7])[CH2:2][CH2:3][CH3:4].C(=O)([O-])[O-].[K+].[K+].[CH2:19](Br)[CH:20]=[CH2:21]>CO>[CH2:21]([N:5]([CH2:1][CH2:2][CH2:3][CH3:4])[S:6]([C:9]([F:12])([F:10])[F:11])(=[O:7])=[O:8])[CH:20]=[CH2:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7841Allyl bromideHCID 11430Potassium CarbonateHCID 20566739N-Butyl-1,1,1-trifluoromethanesulfonamide

생성물 1

HCID 20566762HCID 20566762, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of N-butyltrifluoromethanesulfonamide (62.0 g, 0.302 mole), potassium carbonate (45.54 g, 0.330 mole) and methanol (250 ml) was refluxed with stirring for two hours. Allyl bromide (39.93 g, 0.330 mole) was then added and this mixture stirred under reflux for 24 hours, cooled, filtered, and the solvent evaporated in vacuo. The residue was fractionally distilled yielding 37.0 g (b.p. of 53°-58° C. at 0.07 torr) of the desired compound, N-allyl-N-butyltrifluoromethanesulfonamide.

후처리

  1. temperaturewas refluxed
  2. stirringthis mixture stirred
  3. temperatureunder reflux for 24 hours
  4. temperaturecooled
  5. filtrationfiltered
  6. customthe solvent evaporated in vacuo
  7. distillationThe residue was fractionally distilled

출처 및 근거

ORD 기록
ord-a47dfcdbc77f4442a03410e327d1f0ff
출처 데이터셋
uspto-grants-1981_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04293441

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