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2-(Ethylthio)aniline → HCID 118204261, 화합물

HRID 918776
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HRID 918776 반응식
[N+:1]([C:4]1[CH:11]=[C:10]([C:12]([F:15])([F:14])[F:13])[CH:9]=[CH:8][C:5]=1[CH:6]=O)([O-:3])=[O:2].[CH2:16]([S:18][C:19]1[CH:25]=[CH:24][CH:23]=[CH:22][C:20]=1[NH2:21])[CH3:17]>C1(C)C=CC=CC=1>[CH2:16]([S:18][C:19]1[CH:25]=[CH:24][CH:23]=[CH:22][C:20]=1[N:21]=[CH:6][C:5]1[CH:8]=[CH:9][C:10]([C:12]([F:15])([F:14])[F:13])=[CH:11][C:4]=1[N+:1]([O-:3])=[O:2])[CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 101490092-(Ethylthio)anilineHCID 111603052-Nitro-4-(trifluoromethyl)benzaldehyde

생성물 1

HCID 118204261HCID 118204261, 화합물수율 96.3%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A mixture of 500 mg of 2-nitro-4-trifluoromethylbenzaldehyde, 349 mg of 2-(ethylsulfanyl)aniline and 4 ml of toluene was refluxed for 4 hours and then concentrated under reduced pressure. The resulting residue was washed with t-butyl methyl ether to obtain 777 mg of (2-ethylsulfanylphenyl) (2-nitro-4-trifluoromethylbenzylidene)amine.

후처리

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  • temperaturewas refluxed for 4 hours
  • concentrationconcentrated under reduced pressure
  • washThe resulting residue was washed with t-butyl methyl ether
  • 출처 및 근거

    ORD 기록
    ord-d792b151c9554b06a958cb3a92d649c3
    출처 데이터셋
    uspto-grants-2016_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09271500B2

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