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Citric Acid → 2-Amino-3-nitrobenzoic acid

HRID 1470653
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반응식

HRID 1470653 반응식
[N+:1]([C:4]1[CH:5]=[CH:6][CH:7]=[C:8]2[C:12]=1[NH:11]C(=O)[C:9]2=[O:14])([O-:3])=[O:2].OO.C(O)(=O)CC(CC(O)=O)(C(O)=O)[OH:20]>[OH-].[Na+]>[NH2:11][C:12]1[C:4]([N+:1]([O-:3])=[O:2])=[CH:5][CH:6]=[CH:7][C:8]=1[C:9]([OH:14])=[O:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 311Citric AcidHCID 784Hydrogen PeroxideHCID 38583087-nitro-2,3-dihydro-1H-indole-2,3-dione

생성물 1

HCID 2196332-Amino-3-nitrobenzoic acid수율 70%

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

실험 절차

To a ice cold solution of 7-nitro-1H-indole-2,3-dione (9 g, 47 mmol) in 2 M aqueous sodium hydroxide (50 mL), an aq. solution of 30% hydrogen peroxide (9 mL) was added drop wise. The mixture was warmed to room temperature and stirred overnight. The resulting mixture was carefully acidified by the addition of an aq. saturated citric acid solution. The solid precipitate was collected by filtration, washed with water and dried in a vacuum oven to get 6 g of the required product as a yellow coloured solid (70%).

후처리

  1. filtrationThe solid precipitate was collected by filtration
  2. washwashed with water
  3. customdried in a vacuum oven

출처 및 근거

ORD 기록
ord-f5f2da426de24df18e2ee56633533e4e
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09006454B2

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