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

Isodecanol → (2E)-2-Bromo-2-butenedioic acid

HRID 1656666
노트
인쇄 미리보기

반응식

HRID 1656666 반응식
[Br:1][C:2]1[C:3]([O:5][C:6](=[O:8])[CH:7]=1)=[O:4].C([OH:19])CCCCCCC(C)C>C1(C)C=CC=CC=1>[Br:1]/[C:2](=[CH:7]/[C:6]([OH:5])=[O:8])/[C:3]([OH:19])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 32898IsodecanolHCID 800273-Bromo-2,5-furandione

생성물 1

HCID 5358119(2E)-2-Bromo-2-butenedioic acid수율 260.6%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

Bromomaleic anhydride (19.5 g), isodecanol (69.5 g) p-toluene sulphonic acid (2 g) and toluene (70 ml) were stirred and boiled under reflux below a Dean-Stark trap of volume 15 ml for 2.5 hours. The solution was then cooled with petroleum ether and the petroleum ether solution was washed with water. The solvent and excess isodecanol were distilled under reduced pressure, finally at 100°/0.2 mm of mercury pressure, leaving the bis(isodecyl)ester of bromomaleic acid (56 g) as an oil with an estimated purity by gas chromatography of 96%.

후처리

  1. temperatureunder reflux below a Dean-Stark trap of volume 15 ml for 2.5 hours
  2. washthe petroleum ether solution was washed with water
  3. distillationThe solvent and excess isodecanol were distilled under reduced pressure, finally at 100°/0.2 mm of mercury pressure

출처 및 근거

ORD 기록
ord-5893f884ce5b44b6bbe4d8042f3cff83
출처 데이터셋
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05254695

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트