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2-(2-chloro-4-nitrophenoxy)naphthalene → 3-chloro-4-(2-naphthyloxy)aniline

HRID 1278168
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반응식

HRID 1278168 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([N+:19]([O-])=O)[CH:5]=[CH:6][C:7]=1[O:8][C:9]1[CH:18]=[CH:17][C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=1.[H][H]>C1C=CC=CC=1.C(O)C.[Pt](=O)=O>[Cl:1][C:2]1[CH:3]=[C:4]([CH:5]=[CH:6][C:7]=1[O:8][C:9]1[CH:18]=[CH:17][C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=1)[NH2:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 9215882-(2-chloro-4-nitrophenoxy)naphthaleneHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 34512803-chloro-4-(2-naphthyloxy)aniline수율 60.1%

시약·촉매·용매 3

HCID 345198Adams' catalyst촉매HCID 241Benzene용매HCID 702Ethanol용매

실험 절차

3-Chloro-4-(2-naphthyloxy)nitrobenzene (14.8 g) and platinum dioxide (0.1 g) were suspended in a mixture of benzene and ethanol (1:1) (200 ml), and hydrogenation was carried out until 3.2 liters of hydrogen were absorbed. After removal of the solvent from the reaction mixture by distillation under reduced pressure, the residue was distilled in vacuo to give 3-chloro-4-(2-naphthyloxy)aniline (8 g) as a fraction boiling at 173° to 198° C./0.2 to 0.3 mmHg. M.P., 67°-69° C.

후처리

  1. customwere absorbed
  2. customAfter removal of the solvent from the reaction mixture
  3. distillationby distillation under reduced pressure
  4. distillationthe residue was distilled in vacuo

출처 및 근거

ORD 기록
ord-efc47d8e54434ed28e9794fd7e8a14ce
출처 데이터셋
uspto-grants-1981_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04280835

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