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

1-(3-Chlorophenyl)ethanone → Benzenemethanol, 3-chloro-alpha,alpha-dimethyl-

HRID 2177026
노트
인쇄 미리보기

반응식

HRID 2177026 반응식
[CH3:1][Mg]Br.[CH3:4][C:5]([C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([Cl:13])[CH:8]=1)=[O:6]>CCOCC>[Cl:13][C:9]1[CH:8]=[C:7]([C:5]([OH:6])([CH3:1])[CH3:4])[CH:12]=[CH:11][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 149331-(3-Chlorophenyl)ethanoneHCID 178418573HCID 178418573, 화합물

생성물 1

HCID 593110Benzenemethanol, 3-chloro-alpha,alpha-dimethyl-수율 93.6%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

Methylmagnesium bromide (3.6 mL, 10.67 mmol, Aldrich, 3 M solution in ether) was added to a cooled (−10° C.) solution of 3-chloroacetophenone (1.5 g, 9.7 mmol) in anhydrous ether slowly over 30 min. After complete addition, the reaction mixture was slowly warmed to room temperature, stirred for 18 hours. Again cooled (−5° C.), than quenched with sat. ammonium chloride solution over 30 min. The reaction mixture was extracted with ether, dried, filtered and concentrated to afford 1.55 g of 2-(3-chlorophenyl)propan-2-ol.

후처리

  1. additionAfter complete addition
  2. temperatureAgain cooled (−5° C.)
  3. customthan quenched with sat. ammonium chloride solution over 30 min
  4. extractionThe reaction mixture was extracted with ether
  5. customdried
  6. filtrationfiltered
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-1adb0086d2fc49b899c743659e764a8b
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09067897B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트