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

(4-Chloro-3-methoxyphenyl)methanol → 4-Chloro-3-methoxybenzaldehyde

HRID 38156
노트
인쇄 미리보기

반응식

HRID 38156 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][OH:9])=[CH:4][C:3]=1[O:10][CH3:11]>C1C=CC=CC=1.O=[Mn]=O>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]=[O:9])=[CH:4][C:3]=1[O:10][CH3:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 10910038(4-Chloro-3-methoxyphenyl)methanol

생성물 1

HCID 129097254-Chloro-3-methoxybenzaldehyde수율 89.7%

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매HCID 241Benzene용매

실험 절차

To a solution of (4-chloro-3-methoxyphenyl)methan-1-ol (5.08 g, 29.4 mmol) in benzene (120 mL) was added MnO2 (5.65 g, 65 mmol). The reaction mixture was refluxed for 17 hr, chilled, and filtered through Celite, washing the cake with CH2Cl2 (300 mL). The filtrate was concentrated in vacuo to give 4-chloro-3-methoxybenzaldehyde (4.5 g, 89%).

후처리

  1. temperatureThe reaction mixture was refluxed for 17 hr
  2. temperaturechilled
  3. filtrationfiltered through Celite
  4. washwashing the cake with CH2Cl2 (300 mL)
  5. concentrationThe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-f074e120e9b04d9f9e37f175fd9d00c9
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08524721B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트