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Aniline → 1-Naphthol

HRID 850217
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인쇄 미리보기

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HRID 850217 반응식
N[C:2]1[CH:11]=[C:10](S(O)(=O)=O)[CH:9]=[C:8]2[C:3]=1[C:4]([OH:20])=[CH:5][C:6](S(O)(=O)=O)=[CH:7]2.ClC1N=C(Cl)N=C(Cl)N=1.NC1C=CC=CC=1>>[CH:10]1[CH:11]=[CH:2][C:3]2[C:8](=[CH:7][CH:6]=[CH:5][C:4]=2[OH:20])[CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6115AnilineHCID 7009H acidHCID 7954Cyanuric chloride

생성물 1

HCID 70051-Naphthol

실험 절차

In an aqueous solvent, 31.9 parts of 5-amino-4-hydroxynaphthalene-2,7-disulfonic acid was condensed with 18.4 parts of 2,4,6-trichloro-s-triazine according to a normal method and the resultant condensate was condensed with 28.1 parts of 3-(2-sulfate ethylsulfonyl)aniline according to a normal method. The product thus obtained was condensed with 9.3 parts of aniline according to a normal method to obtain a naphthol derivative.

후처리

  1. customThe product thus obtained

출처 및 근거

ORD 기록
ord-b54a03377a9d4d37853de6453c6ef1ab
출처 데이터셋
uspto-grants-2000_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06015885

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