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4-Fluorophenyl isocyanate → 1-Methyl-beta-oxo-alpha-(p-fluorophenylcarbamoyl)-2-pyrrolpropionitrile

HRID 127586
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HRID 127586 반응식
[CH3:1][N:2]1[CH:6]=[CH:5][CH:4]=[C:3]1[C:7](=[O:11])[CH2:8][C:9]#[N:10].[F:12][C:13]1[CH:18]=[CH:17][C:16]([N:19]=[C:20]=[O:21])=[CH:15][CH:14]=1>C1(C)C=CC=CC=1.C(N(CC)CC)C>[CH3:1][N:2]1[CH:6]=[CH:5][CH:4]=[C:3]1[C:7](=[O:11])[CH:8]([C:20](=[O:21])[NH:19][C:16]1[CH:17]=[CH:18][C:13]([F:12])=[CH:14][CH:15]=1)[C:9]#[N:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 709554-Fluorophenyl isocyanateHCID 27771703-(1-Methyl-1H-pyrrol-2-yl)-3-oxopropanenitrile

생성물 1

HCID 202854081-Methyl-beta-oxo-alpha-(p-fluorophenylcarbamoyl)-2-pyrrolpropionitrile

시약·촉매·용매 2

HCID 1140Toluene용매HCID 8471Triethylamine용매

실험 절차

To the suspension of 4.0 g of 1-methyl-β-oxo-2-pyrrolpropionitrile in 70 ml of toluene and 3.2 g of triethylamine, 3.7 g of p-fluorophenylisocyanate are added while stirring. The mixture is warmed on the steam cone until dissolution and the red-brown solution is allowed to stand overnight at room temperature. It is evaporated on the steam cone, the residue taken up in methanol and the solution poured into the mixture of 8 ml of 5 N hydrochloric acid and 300 ml of water. The precipitated crystals are collected, washed with water, dried, triturated with methanol and recrystalllized from ethyl acetate, to yield the 1-methyl-β-oxo-α-(p-fluorophenylcarbamoyl)-2-pyrrolpropionitrile melting at 198°-199°.

후처리

  1. additionare added
  2. temperatureThe mixture is warmed on the steam cone until dissolution
  3. customIt is evaporated on the steam cone
  4. additionthe solution poured into the mixture of 8 ml of 5 N hydrochloric acid and 300 ml of water
  5. customThe precipitated crystals are collected
  6. washwashed with water
  7. customdried
  8. customtriturated with methanol

출처 및 근거

ORD 기록
ord-2f64fd19d21947a0b715b1e90e45cedb
출처 데이터셋
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04256759

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