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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Nitric Acid → 2-Naphthalenecarboxylic acid, 1-hydroxy-4-nitro-, phenyl ester

HRID 2350842
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인쇄 미리보기

반응식

HRID 2350842 반응식
[N+:1]([O-:4])(O)=[O:2].[O:5]([C:12]([C:14]1[CH:23]=[CH:22][C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[C:15]=1[OH:24])=[O:13])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1>C(Cl)(Cl)Cl>[N+:1]([C:22]1[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[C:15]([OH:24])=[C:14]([C:12]([O:5][C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=2)=[O:13])[CH:23]=1)([O-:4])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric Acid2회HCID 67236Phenyl 1-hydroxy-2-naphthoate

생성물 1

HCID 1033292-Naphthalenecarboxylic acid, 1-hydroxy-4-nitro-, phenyl ester수율 62%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

12 ml of fuming nitric acid (d=1.5) was added dropwise to a solution of 53 g of 2-phenoxycarbonyl-1-naphthol dissolved in 200 ml of chloroform was added dropwise 12 cc of fuming nitric acid (d=1.5) at 10° C. to 30° C. After 30 minutes, the precipitated crystals were filtered, washed well with cooled chloroform to obtain the desired product at a yield of 62%. The product had m.p. of 157° C., and was confirmed by NMR, Mass spectra.

후처리

  1. filtrationthe precipitated crystals were filtered
  2. washwashed well with cooled chloroform

출처 및 근거

ORD 기록
ord-ab1b48f1ee9b47608c0788d370089e11
출처 데이터셋
uspto-grants-1989_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04871655

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