Diphenyl-o-tolylphosphine → [(2-Methylphenyl)diphenylphosphoranylidene]carbamic acid, ethyl ester

HRID 35513노트

반응식

HRID 35513 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[P:8]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[C:21]([N:26]=[N+]=[N-])(=[O:25])[O:22][CH2:23][CH3:24]>CCOCC>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[P:8](=[N:26][C:21](=[O:25])[O:22][CH2:23][CH3:24])([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1

참가 물질

4

반응물 2

HCID 80040Diphenyl-o-tolylphosphineHCID 11819065Ethyl azidoformate

생성물 1

HCID 14280265[(2-Methylphenyl)diphenylphosphoranylidene]carbamic acid, ethyl ester

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

A solution of 1.0 g of (2-methylphenyl)diphenylphosphine in 30 ml of ether was treated with 4 ml of 1M ethyl carbonazidate in ether. The mixture was allowed to stand 48 hours, then repeatedly concentrated and finally treated with fresh ether and refrigerated, giving 930 mg of the desired compound, mp 113°-114° C.

후처리

  1. concentrationrepeatedly concentrated
  2. additionfinally treated with fresh ether

출처 및 근거

ORD 기록
ord-af062f23429c46f4a68a088369966996
출처 데이터셋
uspto-grants-1988_08
특허 번호
US04767749

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