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

Methanol → HCID 20363198, 화합물

HRID 918242
노트
인쇄 미리보기

반응식

HRID 918242 반응식
[S:1]([C:5]1[C:6]([O:8][C:9](=[O:11])[CH:10]=1)=[O:7])([OH:4])(=[O:3])=[O:2].[CH3:12][O-:13].[Na+:14].C[OH:16]>>[CH3:12][O:13][CH:10]([CH:5]([S:1]([OH:4])(=[O:3])=[O:2])[C:6]([O-:16])=[O:7])[C:9]([O-:8])=[O:11].[Na+:14].[Na+:14].[Na+:14]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 887Methanol2회HCID 10942334Sodium MethoxideHCID 12479880Sulfomaleic anhydride

생성물 1

HCID 20363198HCID 20363198, 화합물

반응 조건

온도
80 °C

실험 절차

Sulfomaleic anhydride, 3.9 gm, was dissolved in 25 ml of methanol and refluxed for 5 hours. Then, 24 gm of 25% sodium methoxide in methanol was added and the solution was refluxed for 2 hours. The methanol was then evaporated and the residue was dissolved in 100 ml of water and heated for 1 hour at 80°C. The solution was then decolorized with 5 gm of charcoal, filtered and evaporated. The crude residue of trisodium α-methoxy-β-sulfosuccinate was purified by trituration with acetic acid and then filtered, washed with acetone and dried.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperaturerefluxed for 5 hours
  2. temperaturethe solution was refluxed for 2 hours
  3. customThe methanol was then evaporated
  4. dissolutionthe residue was dissolved in 100 ml of water
  5. filtrationfiltered
  6. customevaporated
  7. customThe crude residue of trisodium α-methoxy-β-sulfosuccinate was purified by trituration with acetic acid
  8. filtrationfiltered
  9. washwashed with acetone
  10. customdried

출처 및 근거

ORD 기록
ord-4ca863efe4cf41889d4e2b76a10af3c7
출처 데이터셋
uspto-grants-1976_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03970653

반응 노트

불러오는 중…