1-Naphthylamine → Hydrazine, 1-naphthalenyl-

HRID 962754

반응식

HRID 962754 반응식
[N:1]([O-])=O.[Na+].[C:5]1([NH2:15])[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=[CH:7][CH:6]=1>O.Cl>[C:5]1([NH:15][NH2:1])[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=[CH:7][CH:6]=1

참가 물질

5

실험 절차

Sodium nitrite (4.8 g) in water (20 ml) was added over 15 minutes to a stirred ice-cold suspension of 1-naphthylamine (9.58 g) in 6M hydrochloric acid (80 ml). After an additional 30 minutes in the ice bath, stannous chloride (44.5 9) in 6M hydrochloric acid (80 ml) was added slowly and the resulting suspension was stirred at O0 for 3 hr. The resulting solid was filtered off and dissolved in a mixture of 40% potassium hydroxide solution (100 ml) and ethyl acetate (150 ml). The organic layer was separated and the aqueous layer was extracted with ethyl acetate (3×100 ml). The combined organic extracts were dried and concentrated under reduced pressure to afford the title compound as a purple solid (10.58 g Rf= 0.1 in EA/CH (1/4)).

후처리

  1. filtrationThe resulting solid was filtered off
  2. dissolutiondissolved in a mixture of 40% potassium hydroxide solution (100 ml) and ethyl acetate (150 ml)
  3. customThe organic layer was separated
  4. extractionthe aqueous layer was extracted with ethyl acetate (3×100 ml)
  5. customThe combined organic extracts were dried
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-e369363131c84756815218413a02911b
출처 데이터셋
uspto-grants-1998_06
특허 번호
US05760059

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