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

HCID 19759911, 화합물 → HCID 19759872, 화합물

HRID 1586865
노트
인쇄 미리보기

반응식

HRID 1586865 반응식
[S:1]1[C:5]2S[CH2:7][CH2:8][C:4]=2[CH:3]=[C:2]1[C:9]([OH:11])=[O:10].O[O:13][S:14]([O-:16])=O.[K+]>O>[S:1]1[C:5]2[S:14](=[O:16])(=[O:13])[CH2:7][CH2:8][C:4]=2[CH:3]=[C:2]1[C:9]([OH:11])=[O:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 19759911HCID 19759911, 화합물HCID 23707502Potassium hydroxy sulfite

생성물 1

HCID 19759872HCID 19759872, 화합물수율 68%

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
60 °C

실험 절차

4,5-Dihydrothieno[2,3-b]thiophene-2-carboxylic acid (88.3 g, 0.474 mol) was added to a solution of Oxone® (730 g, 1.18 mol) in water (3.0 L), and the resulting suspension heated on a steam bath for 1 hour. During this time the solids dissolved to give a clear yellow solution. The reaction was cooled to 60° C. and filtered. The filtrate was extracted four times with ethyl acetate (6 L total) and the combined extracts washed with saturated brine and dried over magnesium sulfate. The solution was filtered and concentrated in vacuo to give the title compound as a yellow solid (70 g, 68%). Recrystallization from dichloroethane gave an off-white powder, mp=227°-230° C. Anal. Calc. for C7H6O4S2 : C, 38.52; H, 2.77. Found: C, 38.53; H, 2.61.

후처리

  1. temperaturethe resulting suspension heated on a steam bath for 1 hour
  2. dissolutionDuring this time the solids dissolved
  3. customto give a clear yellow solution
  4. filtrationfiltered
  5. extractionThe filtrate was extracted four times with ethyl acetate (6 L total)
  6. washthe combined extracts washed with saturated brine
  7. dry with materialdried over magnesium sulfate
  8. filtrationThe solution was filtered
  9. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-ff5d46ff51a046d796efe960f468e37d
출처 데이터셋
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05216020

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트