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

Methyl 3-[2-[(1R)-1-(((2R)-oxiranyl)methoxy)ethyl]phenyl]acrylate → methyl 3-[2-[(1R)-1-(((2R)-oxiranyl)methoxy)ethyl]phenyl]propionate

HRID 1181587
노트
인쇄 미리보기

반응식

HRID 1181587 반응식
[O:1]1[CH2:3][C@@H:2]1[CH2:4][O:5][C@@H:6]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[CH:14]=[CH:15][C:16]([O:18][CH3:19])=[O:17])[CH3:7]>CO>[O:1]1[CH2:3][C@@H:2]1[CH2:4][O:5][C@@H:6]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[CH2:14][CH2:15][C:16]([O:18][CH3:19])=[O:17])[CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 86605593Methyl 3-[2-[(1R)-1-(((2R)-oxiranyl)methoxy)ethyl]phenyl]acrylate

생성물 1

HCID 58662605methyl 3-[2-[(1R)-1-(((2R)-oxiranyl)methoxy)ethyl]phenyl]propionate수율 87.5%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Methyl 3-[2-[(1R)-1-(((2R)-oxiranyl)methoxy)ethyl]phenyl]acrylate (330 mg) obtained in Step 2 was dissolved in methanol (10 ml), 5% rhodium-alumina (43 mg) was added, and the mixture was hydrogenated at atmospheric pressure overnight. The reaction mixture was filtered through Celite, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1) to give the title compound (291 mg).

후처리

  • customwas hydrogenated at atmospheric pressure overnight
  • filtrationThe reaction mixture was filtered through Celite
  • concentrationconcentrated under reduced pressure
  • customThe obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1)
  • 출처 및 근거

    ORD 기록
    ord-9d54567fe5574bd0b853fe09ce4a243e
    출처 데이터셋
    uspto-grants-2007_10
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07285572B2

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트