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Hydrochloric Acid → 8-nitro-2-(3-(trifluoromethyl)phenyl)quinolin-4(1H)-one

HRID 520460
노트
인쇄 미리보기

반응식

HRID 520460 반응식
[N+:1]([C:4]1[CH:5]=[CH:6][CH:7]=[C:8]2[C:13]=1[NH:12][C:11]([C:14]1[CH:19]=[CH:18][CH:17]=[C:16]([C:20]([F:23])([F:22])[F:21])[CH:15]=1)=[C:10](C(OCC)=O)[C:9]2=[O:29])([O-:3])=[O:2].Cl>O1CCOCC1>[N+:1]([C:4]1[CH:5]=[CH:6][CH:7]=[C:8]2[C:13]=1[NH:12][C:11]([C:14]1[CH:19]=[CH:18][CH:17]=[C:16]([C:20]([F:23])([F:21])[F:22])[CH:15]=1)=[CH:10][C:9]2=[O:29])([O-:3])=[O:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 58552877Ethyl 8-nitro-4-oxo-2-(3-(trifluoromethyl)phenyl)-1,4-dihydroquinoline-3-carboxylate

생성물 1

HCID 585529228-nitro-2-(3-(trifluoromethyl)phenyl)quinolin-4(1H)-one수율 86%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

반응 조건

온도
190 °C

실험 절차

A microwave vial was charged with of 8-nitro-4-oxo-2-(3-(trifluoromethyl)phenyl)-1,4-dihydroquinoline-3-carboxylate 36 (1.0 g, 2.46 mmol), dioxane (8 mL) and 1N HCl (4 mL). The reaction mixture was heated at 190° C. in the microwave for 50 min. The volatiles were evaporated and the residue dried under vacuum to give 37 (707 mg, 86% yield).

후처리

  1. customThe volatiles were evaporated
  2. customthe residue dried under vacuum

출처 및 근거

ORD 기록
ord-811edc9f185f4f15bfb06c914ca0523f
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09326986B2

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