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

Ethyl 3-[(4-bromo-3-methoxyphenyl)amino]-3-phenylacrylate → HCID 57617105, 화합물

HRID 1879271
노트
인쇄 미리보기

반응식

HRID 1879271 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[CH:10][C:11]([O:13]CC)=O)=[CH:4][C:3]=1[O:22][CH3:23]>C1C=CC(C2C=CC=CC=2)=CC=1.C1C=CC(OC2C=CC=CC=2)=CC=1>[Br:1][C:2]1[CH:7]=[C:6]2[C:5](=[CH:4][C:3]=1[O:22][CH3:23])[NH:8][C:9]([C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1)=[CH:10][C:11]2=[O:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 58005168Ethyl 3-[(4-bromo-3-methoxyphenyl)amino]-3-phenylacrylate

생성물 1

HCID 57617105HCID 57617105, 화합물수율 86%

시약·촉매·용매 1

HCID 246701,1'-Biphenyl, mixt. with 1,1'-oxybis(benzene)용매3회

반응 조건

온도
300 °C

실험 절차

DOWTHERM A (0.19 M) was heated to reflux (˜300° C.). A mixture of the product 113 in DOWTHERM A (2.5 M) was added to the heated DOWTHERM A solution portionwise. The mixture was stirred at reflux for 1 h after the addition was complete. The mixture was cooled to RT, filtered, and the solid was washed with hexane to give the title compound 114 (86%). 1H NMR (DMSO-d6) (ppm) 11.69 (s, 1H), 8.19 (s, 1H), 7.82 (m, 2H), 7.59 (m, 3H), 7.35 (s, 1H), 6.33 (s, 1H), 3.96 (s, 3H).

후처리

  1. temperatureat reflux for 1 h
  2. additionafter the addition
  3. temperatureThe mixture was cooled to RT
  4. filtrationfiltered
  5. washthe solid was washed with hexane

출처 및 근거

ORD 기록
ord-591e420a93e4465f9399c4b121b16460
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08314062B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트