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Hydroxyphenylacetic acid → 1-(2-Hydroxy-4-methoxyphenyl)-2-(4-hydroxyphenyl)ethanone

HRID 1296685
노트
인쇄 미리보기

반응식

HRID 1296685 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([OH:9])[CH:6]=[CH:7][CH:8]=1.[OH:10][C:11]1[CH:16]=[CH:15][C:14]([CH2:17][C:18](O)=[O:19])=[CH:13][CH:12]=1.B(F)(F)F.CCOCC>ClC1C=CC=CC=1>[OH:9][C:5]1[CH:4]=[C:3]([O:2][CH3:1])[CH:8]=[CH:7][C:6]=1[C:18](=[O:19])[CH2:17][C:14]1[CH:15]=[CH:16][C:11]([OH:10])=[CH:12][CH:13]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 127Hydroxyphenylacetic acidHCID 8000Boron trifluoride etherateHCID 90073-Methoxyphenol

생성물 1

HCID 149200561-(2-Hydroxy-4-methoxyphenyl)-2-(4-hydroxyphenyl)ethanone

시약·촉매·용매 1

HCID 7964Chlorobenzene용매

반응 조건

온도
7.5 °C

실험 절차

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

A suspension of 3-methoxyphenol (44.69 kg, 360 mol) and 4-hydroxyphenylacetic acid (68.5 kg, 450 mol) in 144 L of chlorobenzene was purged with nitrogen gas. Boron trifluoride diethyl etherate (177 L, 1440 mol) was added at 20 to 25° C. The resultant suspension was heated to 80° C., stirred for 4 to 5 h, cooled to 5 to 10° C. and stirred overnight.

후처리

  1. customwas purged with nitrogen gas
  2. stirringstirred overnight

출처 및 근거

ORD 기록
ord-8e508067939f4ac5a45a7ebddbf1c416
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07247646B2

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