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

HRID 426915
ノート
印刷プレビュー

反応式

HRID 426915 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-f4f3e96a7eab416fb23ac8157a7cd070
出典データセット
uspto-grants-1979_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04172093

反応ノート

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