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Anthranilic Acid → 2-(Nitroamino)benzoic acid

HRID 334501
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HRID 334501 반응식
S(=O)(=O)(O)O.[NH2:6][C:7]1[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=1[C:9]([OH:11])=[O:10].[N+:16]([O-])([OH:18])=[O:17].[NH4+].[OH-]>>[N+:16]([NH:6][C:7]1[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=1[C:9]([OH:11])=[O:10])([O-:18])=[O:17]
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참가 물질

5

반응물 4

HCID 227Anthranilic AcidHCID 944Nitric AcidHCID 1118Sulfuric Acid2회HCID 14923Ammonium Hydroxide

생성물 1

HCID 215441192-(Nitroamino)benzoic acid수율 75.4%

실험 절차

To a solution of concentrated sulfuric acid (2 mL) was slowly added 2-aminobenzoic acid (CXXIV) (1.0 g, 7.24 mmol). A mixture of concentrated sulfuric acid (1.5 mL) and fuming nitric acid (1.5 mL) was then slowly added and the reaction was stirred at room temperature overnight. The reaction mixture was poured into crushed ice and treated with aqueous NH4OH until pH 3.0. The yellow-orange solid was washed with cold water and dried to produce 2-(nitroamino)benzoic acid (CXXV) as a yellow solid (1.0 g, 5.46 mmol, 75.4% yield). The crude product was used for the next step without further purification. ESIMS found for C7H6N2O4 m/z 183.9 (M+H).

후처리

  1. additionwas then slowly added
  2. additionThe reaction mixture was poured
  3. custominto crushed ice
  4. washThe yellow-orange solid was washed with cold water
  5. customdried

출처 및 근거

ORD 기록
ord-d90cb9f046a74881894c4521acd0edb2
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08883822B2

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