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Sodium Nitrate → 5'-Hydroxy-spiro(cyclopentane-1,1'-indan)-3'-one

HRID 426915
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HRID 426915 반응식
N[C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7]1([CH2:14][CH2:13][CH2:12][CH2:11]1)[CH2:6][C:5]2=[O:15].[N+]([O-])([O-])=[O:17].[Na+]>O>[OH:17][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7]1([CH2:14][CH2:13][CH2:12][CH2:11]1)[CH2:6][C:5]2=[O:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24268Sodium NitrateHCID 203884255'-Amino-spiro(cyclopentane-1,1'-indan)-3'-one

생성물 1

HCID 203884005'-Hydroxy-spiro(cyclopentane-1,1'-indan)-3'-one수율 98.9%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 5'-amino-spiro(cyclopentane-1,1'-indan)-3'-one (20.1 g; 0.1 mole) 2 N sulphoric acid (150 ml) and ice (30 g) is diazotised at about +5° C. with a solution of sodium nitrate (11 g) in water (25 ml). The solution is filtrated and poured in boiling mixture of 100 ml of water and 10 ml of conc. sulphuric acid. The boiling is continued until the development of nitrogen gas ceases, after which the mixture is chilled and the solid, dark brown substance is filtered off. After drying there are obtained 20 g of a crude product, which is recrystallized from trichloroethylene. Yield 12 g of a light powder of mp. 145° C. 4 g of the substance can be recovered from the mother liquid by means of extraction with 2 N sodium hydroxide and subsequent precipitation with 2 N hydrochloric acid.

후처리

  1. filtrationThe solution is filtrated
  2. additionpoured
  3. additionmixture of 100 ml of water and 10 ml of conc. sulphuric acid
  4. temperatureafter which the mixture is chilled
  5. filtrationthe solid, dark brown substance is filtered off
  6. customAfter drying there

출처 및 근거

ORD 기록
ord-f4f3e96a7eab416fb23ac8157a7cd070
출처 데이터셋
uspto-grants-1979_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04172093

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