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Sulfuric Acid → 8-Azidonaphthalen-1-ol

HRID 1580533
ノート
印刷プレビュー

反応式

HRID 1580533 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 215619898-Azidonaphthalen-1-ol

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-8665a939ec6448d6ad4df13c68c0dfdf
出典データセット
uspto-grants-1976_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03933497

反応ノート

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