Acetonitrile → HCID 178421665、化合物

HRID 1737146ノート

反応式

HRID 1737146 の反応式
[OH:1][C:2]1[C:3](=[O:13])[C:4]2[C:9]([C:10](=[O:12])[CH:11]=1)=[CH:8][CH:7]=[CH:6][CH:5]=2.S(O[O-])([O-])(=O)=O.[NH4+].[NH4+].[C:22](#N)[CH3:23]>O.C(OCC)C.[N+]([O-])([O-])=O.[Ag+]>[OH:1][C:2]1[C:3](=[O:13])[C:4]2[C:9]([C:10](=[O:12])[C:11]=1[C:22]1([CH3:23])[CH2:10][CH2:11][CH2:2][CH2:3]1)=[CH:8][CH:7]=[CH:6][CH:5]=2

参加物

7

反応条件

温度
20 °C

実験手順

A 50% excess of this acid was added to a stirred solution of 2-hydroxynaphthalene-1,4-dione (1.00 g, 5.7 mmol), and silver nitrate (600 mg) in a mixture of acetonitrile (20 ml) and water (20 ml) at 65° C. and a solution of ammonium peroxysulphate (1.96 g, 8.6 mmol) in water (10 ml) was slowly added to that over a period of 15 minutes. The mixture was heated for a further hour before cooling to room temperature (about 20° C.) and diluting with diethyl ether (50 ml). The organic phase was separated and washed successively with 25 water, dilute aqueous sodium hydrogen carbonate solution, water and saturated sodium chloride solution before drying over magnesium sulphate as set out in Example 3. Filtration and evaporation of the solvent under reduced pressure followed by silica gel column chromatography using 2:1 petrol:diethyl ether as eluant gave 2-hydroxy-3-(1-methylcyclopentyl)naphthalene-1,4-dione (mp 116-118° C.).

後処理

  1. temperatureThe mixture was heated for a further hour
  2. customThe organic phase was separated
  3. washwashed successively with 25 water, dilute aqueous sodium hydrogen carbonate solution, water and saturated sodium chloride solution
  4. dry with materialbefore drying over magnesium sulphate
  5. filtrationFiltration and evaporation of the solvent under reduced pressure

出典と根拠

ORDレコード
ord-6b7f9a07a2384d09985199932e760a08
出典データセット
uspto-grants-1999_10
特許番号
US05962002

反応ノート

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