홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

O-Cresol → 1,3-Dimethyl-5-(methoxycarbonyl-methylene)-hydantoin

HRID 372160
노트
인쇄 미리보기

반응식

HRID 372160 반응식
[CH3:1][NH:2][C:3]([NH:5][CH3:6])=[O:4].C/[C:8](/[C:14]([O-:16])=O)=[C:9](\C)/[C:10]([O-:12])=[O:11].[C:17]1(C)C(O)=CC=CC=1>ClC1C=CC=CC=1Cl>[CH3:1][N:2]1[C:8](=[CH:9][C:10]([O:12][CH3:17])=[O:11])[C:14](=[O:16])[N:5]([CH3:6])[C:3]1=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 335O-CresolHCID 7293N,N'-DimethylureaHCID 5459894Dimethylmaleate

생성물 1

HCID 540964411,3-Dimethyl-5-(methoxycarbonyl-methylene)-hydantoin

시약·촉매·용매 1

HCID 72391,2-Dichlorobenzene용매

실험 절차

44 g of N,N'-dimethylurea were dissolved in 150 g of o-dichlorobenzene and reacted with 72 g of dimethylmaleate for 2 hours at 180°-185° C after the addition of 25 g of cresol. The solvent was removed from this reaction mixture and the residue was fractionated under vacuum, 85 g (= 85% of the theory) of the desired product distilling over at 0.07 Torr and 128° C. A purified product melting at 49.5° C could be obtained by dissolving the crude product in chloroform and reprecipitating it with ether. The structure of the purified product was confirmed by IR and NMR spectra and by elementary analysis.

후처리

  1. customThe solvent was removed from this reaction mixture
  2. distillationdistilling over at 0.07 Torr and 128° C

출처 및 근거

ORD 기록
ord-57af96b92cdb484db5e792ce9ad2d545
출처 데이터셋
uspto-grants-1978_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04089860

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트