Dinitrofluorobenzene → HCID 4922992, 화합물

HRID 1611881노트

반응식

HRID 1611881 반응식
[N+:1]([C:4]1[CH:9]=[C:8]([N+:10]([O-:12])=[O:11])[CH:7]=[CH:6][C:5]=1F)([O-:3])=[O:2].CN1CCCC1=O.[CH2:21]([NH:24][CH2:25][CH:26]=[CH2:27])[CH:22]=[CH2:23].C(=O)([O-])[O-].[K+].[K+]>O>[CH2:21]([N:24]([CH2:25][CH:26]=[CH2:27])[C:5]1[CH:6]=[CH:7][C:8]([N+:10]([O-:12])=[O:11])=[CH:9][C:4]=1[N+:1]([O-:3])=[O:2])[CH:22]=[CH2:23]

참가 물질

6

반응물 4

HCID 6264DinitrofluorobenzeneHCID 11430Potassium CarbonateHCID 13387N-methyl-2-pyrrolidoneHCID 31279Diallylamine

생성물 1

HCID 4922992HCID 4922992, 화합물수율 110.9%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 2,4-dinitrofluorobenzene (9.3 g, 50 mmol), 1-methylpyrrolidinone (50 mL), diallylamine (5.82 g, 60 mmol) and potassium carbonate (6.9 g, 50 mmol) was stirred at ambient temperature for 1 h. The mixture was poured into water (250 mL) and extracted with ethyl ether. The ether extract was washed with 0.5 N hydrochloric acid, water, and saturated brine solution, and dried over magnesium sulfate. Concentration of the extract gave N,N-diallyl-2,4-dinitrobenzeneamine as a yellow oil (14.6 g).

후처리

  1. extractionextracted with ethyl ether
  2. extractionThe ether extract
  3. washwas washed with 0.5 N hydrochloric acid, water, and saturated brine solution
  4. dry with materialdried over magnesium sulfate

출처 및 근거

ORD 기록
ord-f41eafe73dc54364abdbfcd54f5e3202
출처 데이터셋
uspto-grants-2006_01
특허 번호
US06991834B1

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