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Nitrogen oxide (N2O4) → 3-(4'-Bromophenyl)-2-nitronaphtho-[1,2-b]furan

HRID 224303
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인쇄 미리보기

반응식

HRID 224303 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9]3[CH:20]=[CH:19][C:18]4[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=4)[C:10]=3[O:11][CH:12]=2)=[CH:4][CH:3]=1.[N+:21]([O-:26])([N+]([O-])=O)=[O:22]>ClCCl>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[C:9]3[CH:20]=[CH:19][C:18]4[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=4)[C:10]=3[O:11][C:12]=2[N+:21]([O-:26])=[O:22])=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 25352Nitrogen oxide (N2O4)HCID 155716033-(4'-Bromophenyl)naphtho-[1,2-b]furan

생성물 1

HCID 155716043-(4'-Bromophenyl)-2-nitronaphtho-[1,2-b]furan

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 2 g. of the product of step B in 50 ml. of dichloromethane is treated with 2.0 g. of dinitrogen tetraoxide, and the mixture is stirred at about 20° C. for about 18 hours. The mixture is evaporated, and the residue obtained is recrystallized from aqueous ethanol to provide yellow crystals of 3-(4'-bromophenyl)-2-nitronaphtho-[1,2-b]furan, m.p. 230°-233° C.

후처리

  1. customThe mixture is evaporated
  2. customthe residue obtained
  3. customis recrystallized from aqueous ethanol

출처 및 근거

ORD 기록
ord-8f0246653e0d4b4abe351e69b7395e98
출처 데이터셋
uspto-grants-1980_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04231965

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