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

Sulfuric Acid → methyl (2-oxopropoxy)acetate

HRID 987376
노트
인쇄 미리보기

반응식

HRID 987376 반응식
[CH2:1]([O:4][CH2:5][C:6]([O:8][CH3:9])=[O:7])[C:2]#[CH:3].S(=O)(=O)(O)[OH:11]>CO.C([O-])(=O)C.[Hg+2].C([O-])(=O)C>[O:11]=[C:2]([CH3:3])[CH2:1][O:4][CH2:5][C:6]([O:8][CH3:9])=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 1118Sulfuric AcidHCID 10877131Methyl 2-(prop-2-yn-1-yloxy)acetate

생성물 1

HCID 11701055methyl (2-oxopropoxy)acetate

시약·촉매·용매 2

HCID 15337Mercuric acetate촉매HCID 887Methanol용매

실험 절차

The product from Example 1A (56 g, 0.44 mol) in methanol (1.5 L) was treated with mercury(II) acetate (14 g, 44 mmol), treated with concentrated sulfuric acid (3 mL), refluxed for 1 hour, allowed to cool to ambient temperature, concentrated to a volume of 200 mL, treated with 1M HCl (500 mL) and extracted with dichloromethane (thrice, 300 mL). The combined dichloromethane layers were dried (MgSO4), filtered, concentrated and distilled (65-95° C. at 1 torr) to provide the title compound.

후처리

  1. temperaturerefluxed for 1 hour
  2. concentrationconcentrated to a volume of 200 mL
  3. additiontreated with 1M HCl (500 mL)
  4. extractionextracted with dichloromethane (thrice, 300 mL)
  5. dry with materialThe combined dichloromethane layers were dried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated
  8. distillationdistilled (65-95° C. at 1 torr)

출처 및 근거

ORD 기록
ord-2465d680036b4727a5e734aee66f20ce
출처 데이터셋
uspto-grants-2003_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06632418B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트