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Sulfuric Acid → 8-Azidonaphthalen-1-ol

HRID 1580533
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HRID 1580533 반응식
[N:1]([C:4]1[CH:5]=[CH:6][CH:7]=[C:8]2[C:13]=1[C:12](N)=[CH:11][CH:10]=[CH:9]2)=[N+:2]=[N-:3].S(=O)(=O)(O)[OH:16].N([O-])=O.[Na+]>O>[N:1]([C:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][C:12]=2[OH:16])[CH:7]=[CH:6][CH:5]=1)=[N+:2]=[N-:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1118Sulfuric AcidHCID 120253881-Naphthalenamine, 8-azido-HCID 23668193Sodium Nitrite

생성물 1

HCID 215619898-Azidonaphthalen-1-ol

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A sample of 8-azido-1-naphthylamine (0.368 g., 0.02 mole) was dissolved in warm, dilute sulfuric acid (3 ml. of conc. H2SO4 diluted with 30 ml. of water). The solution was cooled to O°C. and diazotized with a solution of NaNO2 (160 mg., 0.023 mole) in 2 ml. of water. The excess of nitrous acid was destroyed by the addition of urea. The yellow solution of the diazonium salt was diluted with 100 ml. of water and heated at 60°for 1.5 hr. The precipitated material was washed with water, dried and filtered through activated charcoal. Removal of ether left a residue which weighed 35 mg. Recrystallization from petroleum ether gave 1-azido-8-hydroxynaphthalene in the form of pale yellow needles (20 mg., 5.4 percent), m.p. 65°C.-67°C.

후처리

  1. temperaturein warm
  2. temperatureThe solution was cooled to O°C
  3. customThe excess of nitrous acid was destroyed by the addition of urea
  4. additionThe yellow solution of the diazonium salt was diluted with 100 ml
  5. temperatureof water and heated at 60°for 1.5 hr
  6. washThe precipitated material was washed with water
  7. customdried
  8. filtrationfiltered through activated charcoal
  9. customRemoval of ether
  10. waitleft a residue which
  11. customRecrystallization from petroleum ether

출처 및 근거

ORD 기록
ord-8665a939ec6448d6ad4df13c68c0dfdf
출처 데이터셋
uspto-grants-1976_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03933497

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