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Triphosgene → p-(Tetradecyloxy)phenyl isocyanate

HRID 1461918
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인쇄 미리보기

반응식

HRID 1461918 반응식
Cl[C:2](Cl)([O:4]C(=O)OC(Cl)(Cl)Cl)Cl.[CH2:13]([O:27][C:28]1[CH:34]=[CH:33][C:31]([NH2:32])=[CH:30][CH:29]=1)[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]>C(Cl)Cl>[CH2:13]([O:27][C:28]1[CH:34]=[CH:33][C:31]([N:32]=[C:2]=[O:4])=[CH:30][CH:29]=1)[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 94429TriphosgeneHCID 191002p-(n-Tetradecyloxy)phenylamine

생성물 1

HCID 11724283p-(Tetradecyloxy)phenyl isocyanate

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a solution of 8.74 g of triphosgene in 125 ml of methylene chloride cooled to 0° C. is added dropwise a solution of p-(tetradecyloxy)aniline, 7.95 g of 125 ml of methylene chloride over 30 minutes. Stirring at ambient temperature is continued for 4 hours. The solvent is evaporated and the residue stirred with ether and filtered. The cake is washed with additional ether and the combined filtrates evaporated to give the desired product as an oil.

후처리

  1. customThe solvent is evaporated
  2. stirringthe residue stirred with ether
  3. filtrationfiltered
  4. washThe cake is washed with additional ether
  5. customthe combined filtrates evaporated

출처 및 근거

ORD 기록
ord-d97234e6bd784ba9822fddd79537fc57
출처 데이터셋
uspto-grants-1991_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05077409

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