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

Dimethylsulfoxonium methylide → Methyl 2-(4-cyclohexylphenyl)cyclopropanecarboxylate

HRID 446764
노트
인쇄 미리보기

반응식

HRID 446764 반응식
[CH:1]1([C:7]2[CH:12]=[CH:11][C:10](/[CH:13]=[CH:14]/[C:15]([O:17][CH3:18])=[O:16])=[CH:9][CH:8]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:19]S(C)(=O)=C>CS(C)=O>[CH:1]1([C:7]2[CH:8]=[CH:9][C:10]([CH:13]3[CH2:19][CH:14]3[C:15]([O:17][CH3:18])=[O:16])=[CH:11][CH:12]=2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6396768Dimethylsulfoxonium methylideHCID 58358304(E)-methyl 3-(4-cyclohexylphenyl)acrylate

생성물 1

HCID 58358302Methyl 2-(4-cyclohexylphenyl)cyclopropanecarboxylate수율 70.8%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

To a solution of (E)-methyl 3-(4-cyclohexylphenyl)acrylate (200 mg, 0.82 mmol) in DMSO (20 mL) was added freshly prepared Corey's reagent (92 mg, 0.98 mmol) at RT and stirred for 3 h. The reaction was quenched with cold water and then extracted with EtOAc (2×20 mL). The combined organic layers were dried over magnesium sulfate, filtered and then concentrated in vacuo to obtain crude product. The crude material was purified via silica gel column chromatography eluting with 5% EtOAc/95% hexanes to afford methyl 2-(4-cyclohexylphenyl)cyclopropanecarboxylate (150 mg, 47%) as a solid.

후처리

  1. customThe reaction was quenched with cold water
  2. extractionextracted with EtOAc (2×20 mL)
  3. dry with materialThe combined organic layers were dried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customto obtain crude product
  7. customThe crude material was purified via silica gel column chromatography
  8. washeluting with 5% EtOAc/95% hexanes

출처 및 근거

ORD 기록
ord-a9adf2ac06774ad5bee9ead93d52c88d
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08481532B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트