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Triethylamine → (+/-)-5-(2,6-Dichlorophenyl)-3-(3-nitrophenyl)-2-isoxazoline

HRID 2053387
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HRID 2053387 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([C:10](Cl)=[N:11][OH:12])[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].[Cl:14][C:15]1[CH:22]=[CH:21][CH:20]=[C:19]([Cl:23])[C:16]=1[CH:17]=[CH2:18].C(N(CC)CC)C>C1COCC1>[Cl:14][C:15]1[CH:22]=[CH:21][CH:20]=[C:19]([Cl:23])[C:16]=1[CH:17]1[O:12][N:11]=[C:10]([C:6]2[CH:7]=[CH:8][CH:9]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=2)[CH2:18]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471Triethylamine2회HCID 342542,6-DichlorostyreneHCID 2756318alpha-Chloro-3-nitrobenzaldoxime

생성물 1

HCID 69221841(+/-)-5-(2,6-Dichlorophenyl)-3-(3-nitrophenyl)-2-isoxazoline

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

3-Nitro-N-hydroxybenzenecarboximidoyl chloride (1.16 g, 5.78 mmol) and 2,6-dichlorostyrene (1.0 g, 5.78 mmol) were dissolved in anhydrous THF (20 mL) and triethylamine (1.21 mL, 8.67 mmol). Upon addition of triethylamine a while solid formed. After 3 h this solid was collected by filtration under reduced pressure to provide the title compound as a white solid.

후처리

  1. customformed
  2. filtrationAfter 3 h this solid was collected by filtration under reduced pressure

출처 및 근거

ORD 기록
ord-73f9f14d9f514b97b18ad1a80624141f
출처 데이터셋
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07326790B2

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