Propargyl bromide → N-cyano-N-propargyl-3-trifluoromethylaniline

HRID 22033노트

반응식

HRID 22033 반응식
[C:1]([NH:3][C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]([F:13])([F:12])[F:11])[CH:5]=1)#[N:2].C(=O)([O-])[O-].[K+].[K+].[CH2:20](Br)[C:21]#[CH:22]>CC(C)=O>[C:1]([N:3]([CH2:22][C:21]#[CH:20])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]([F:11])([F:12])[F:13])[CH:5]=1)#[N:2]

참가 물질

5

반응물 3

HCID 7842Propargyl bromideHCID 11430Potassium CarbonateHCID 110741023-(Trifluoromethyl)phenylcyanamide

생성물 1

HCID 22416968N-cyano-N-propargyl-3-trifluoromethylaniline수율 63.1%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a solution of N-cyano-3-trifluoromethylaniline (5.0 g) in acetone (100 ml) , potassium carbonate (7.4 g) and propargyl bromide (3.5 g) were added, and the resultant mixture was stirred at room temperature for 10 hours, followed by filtration of the reaction mixture. The solvent was removed from the filtrate by distillation under reduced pressure, and the residue was subjected to column chromatography to give N-cyano-N-propargyl-3-trifluoromethylaniline (3.8 g). The thus obtained N-cyano-N-propargyl-3-trifluoromethylaniline (1 g) and a catalytic amount of triethylamine were dissolved in methanol (30 ml), and the resultant mixture was cooled to 0° C. Hydrogen sulfide was gradually introduced into the mixture for 20 minutes while keeping the temperature at 0° C., followed by introduction of nitrogen gas to remove hydrogen sulfide. The solvent was removed by distillation, and the residue was subjected to column chromatography to give 0.2 g of 2-imino-3-(3-trifluoromethylphenyl)-5-methylenethiazolidine (Compound (ix)).

후처리

  1. filtrationfollowed by filtration of the reaction mixture
  2. customThe solvent was removed from the filtrate by distillation under reduced pressure

출처 및 근거

ORD 기록
ord-f2cfedff3b6a484d9c264a2bada38823
출처 데이터셋
uspto-grants-1995_06
특허 번호
US05426188

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