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

Chlorosulfonic acid → 5-Chlorofuran-2-sulfonyl chloride

HRID 1815631
노트
인쇄 미리보기

반응식

HRID 1815631 반응식
P(Cl)(Cl)(Cl)(Cl)Cl.[Cl:7][S:8]([OH:11])(=O)=[O:9].[Cl:12][C:13]1[O:14][CH:15]=[CH:16][CH:17]=1>>[Cl:12][C:13]1[O:14][C:15]([S:8]([Cl:7])(=[O:11])=[O:9])=[CH:16][CH:17]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 24638Chlorosulfonic acidHCID 24819Phosphorus pentachlorideHCID 1378562-Chlorofuran

생성물 1

HCID 225007325-Chlorofuran-2-sulfonyl chloride수율 360.2%

반응 조건

온도
25 °C

실험 절차

Phosphorus pentachloride (40.53 g, 0.1947 mol) was added portionwise (caution, foaming) over 5 min at 25° C. to chlorosulfonic acid (56.8 g, 32.4 mL, 0.487 mol) and the resulting solution was stirred at 25° C. for 10 min. Then, 2-chlorofuran (20.0 g, 0.1947 mol) was added in one portion and the resulting dark suspension was heated to 55° C. for 1.0 h during which time foaming occurred and subsided. The reaction mixture was then poured onto ice and the resulting suspension was extracted with CH2Cl2 (250 mL). The organic was filtered through a pad of celite, washed with brine (70 mL) and dried over MgSO4. The solvent was removed in vacuo to provide 5-chlorofuran-2-sulfonyl chloride as a black oil (141 g, 36.02%). 1H-NMR (DMSO-d6, 400 MHz) δ 7.05 (d, 1H); 6.35 (d, 1H).

후처리

  1. temperaturethe resulting dark suspension was heated to 55° C. for 1.0 h during which time
  2. additionThe reaction mixture was then poured onto ice
  3. extractionthe resulting suspension was extracted with CH2Cl2 (250 mL)
  4. filtrationThe organic was filtered through a pad of celite
  5. washwashed with brine (70 mL)
  6. dry with materialdried over MgSO4
  7. customThe solvent was removed in vacuo

출처 및 근거

ORD 기록
ord-1ec50ffd973f41099d12f02e0c415586
출처 데이터셋
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06878742B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트