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2-Methoxybenzene-1,3,5-tricarboxylic acid → 2-Hydroxy-1,3,5-benzenetricarboxylic acid

HRID 1038286
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인쇄 미리보기

반응식

HRID 1038286 반응식
C[O:2][C:3]1[C:8]([C:9]([OH:11])=[O:10])=[CH:7][C:6]([C:12]([OH:14])=[O:13])=[CH:5][C:4]=1[C:15]([OH:17])=[O:16]>Br>[OH:2][C:3]1[C:4]([C:15]([OH:17])=[O:16])=[CH:5][C:6]([C:12]([OH:14])=[O:13])=[CH:7][C:8]=1[C:9]([OH:11])=[O:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 234241902-Methoxybenzene-1,3,5-tricarboxylic acid

생성물 1

HCID 234240322-Hydroxy-1,3,5-benzenetricarboxylic acid

시약·촉매·용매 1

HCID 260Hydrogen Bromide용매

반응 조건

온도
150 °C

실험 절차

A mixture of 2-methoxy-benzene-1,3,5-tricarboxylic acid (3) (24 g, 0.1 mol) and 48% HBr (500 mL) was placed in a 1 L bound bottom flask. The reaction mixture was heated to reflux at 150° C. for 48 h. The progress of the deprotection was monitored by proton NMR. When the reaction was complete, the hydrobromic acid was removed under reduced pressure, and the residue was mixed with small amount of water. The deprotected triacid (13) was collected by filtration; yield 17 grams (75%).

후처리

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
  1. temperatureThe reaction mixture was heated
  2. customthe hydrobromic acid was removed under reduced pressure
  3. additionthe residue was mixed with small amount of water
  4. filtrationThe deprotected triacid (13) was collected by filtration

출처 및 근거

ORD 기록
ord-288f256b863b4c629153d32ff79945c7
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08551453B2

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