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Nitric Acid → HCID 66703994, 화합물

HRID 425258
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HRID 425258 반응식
[C:1]([NH:4][C:5]1[CH:14]=[C:13]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([Cl:21])[CH:11]=2)[N:6]=1)(=[O:3])[CH3:2].[N+:22]([O-])([OH:24])=[O:23]>>[C:1]([NH:4][C:5]1[CH:14]=[C:13]([C:15]2[CH:16]=[CH:17][C:18]([N+:22]([O-:24])=[O:23])=[CH:19][CH:20]=2)[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([Cl:21])[CH:11]=2)[N:6]=1)(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 944Nitric AcidHCID 22403906HCID 22403906, 화합물

생성물 1

HCID 66703994HCID 66703994, 화합물

실험 절차

200 mg of 2-acetylamino-6-chloro-4-phenylquinoline were introduced in portions into 4 ml of 100% strength HNO3 at 0° C. and stirred at 0° C. to 5° C. for 30 min, and the reaction mixture was poured into ice-water. Neutralization with 2N NaOH was followed by extraction with ethyl acetate and removal of the solvent by distillation. The solid residue was boiled several times with diisopropyl ether, and the solvent of the filtrate was evaporated until the substance separated out as crystals.

후처리

  1. extractionNeutralization with 2N NaOH was followed by extraction with ethyl acetate and removal of the solvent by distillation
  2. customthe solvent of the filtrate was evaporated until the substance
  3. customseparated out as crystals

출처 및 근거

ORD 기록
ord-f35985a1360342929d19e90d22060180
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08106204B2

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