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

Sulfuryl chloride → 1-Propanone, 2-chloro-2-methyl-1-phenyl-

HRID 1266673
노트
인쇄 미리보기

반응식

HRID 1266673 반응식
[C:1]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)(=[O:5])[CH:2]([CH3:4])[CH3:3].S(Cl)([Cl:15])(=O)=O>CCCCCCC>[Cl:15][C:2]([CH3:4])([CH3:3])[C:1]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24648Sulfuryl chlorideHCID 69144Isobutyrophenone

생성물 1

HCID 819851-Propanone, 2-chloro-2-methyl-1-phenyl-

시약·촉매·용매 1

HCID 8900Heptane용매

실험 절차

Isobutyrophenone (30.0 g, 0.20 mole) was dissolved in heptane (10 ml) and sulfuryl chloride (35 g, 0.26 mole) was added at once. After a few minutes gas evolution occurred. After 3 h of stirring at room temperature the reaction mixture was concentrated. The concentrate was dissolved in heptane (250 ml) and washed with 150 ml of an aqueous 2 wt % sodium bicarbonate solution. After drying over magnesium sulfate the solvent was removed under reduced pressure. The yield of 2-chloro-2-methylpropiophenone was 36.4 g or 98%.

후처리

  1. waitAfter a few minutes gas evolution occurred
  2. concentrationwas concentrated
  3. dissolutionThe concentrate was dissolved in heptane (250 ml)
  4. washwashed with 150 ml of an aqueous 2 wt % sodium bicarbonate solution
  5. dry with materialAfter drying over magnesium sulfate the solvent
  6. customwas removed under reduced pressure

출처 및 근거

ORD 기록
ord-a07e5f5e6b3a40f2bc70bf1e69f1195a
출처 데이터셋
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06548710B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트