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HRID 5002作成日:2026年10月23日

Sodium Bicarbonate → 1-amino-2,3-dihydro-4,6-dimethyl-7-hydroxy-2-phenyl-1H-indene

https://huagongshe.com/ja/reaction/5002

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物2,3-dihydro-4,6-dimethyl-7-hydroxy-2-phenyl-1H-inden-1-one oximeHCID 136342832—
反応物HCID 178418361HCID 178418361—
触媒Platinum oxide (PtO)HCID 82844—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
生成物1-amino-2,3-dihydro-4,6-dimethyl-7-hydroxy-2-phenyl-1H-indeneHCID 14030334—

反応手順

3.00 Grams of 2,3-dihydro-4,6-dimethyl-7-hydroxy-2-phenyl-1H-inden-1-one oxime was dissolved in 55 ml of glacial acetic acid, and this solution was subjected to catalytic hydrogenation in the presence of 0.3 g of platinum oxide at room temperature under 4 atmospheric hydrogen gas pressure. The hydrogenation was terminated at the point when the stoichiometric amount of hydrogen was absorbed. The catalyst was removed by filtration and the filtrate thus obtained was concentrated. The residue thus obtained was dissolved in water and the pH of this solution was adjusted to about pH 8 by adding an aqueous solution of sodium bicarbonate, then extracted with 200 ml of chloroform. The chloroform extract was washed with water, dried with anhydrous magnesium sulfate, then concentrated under a reduced pressure. Recrystallized from ethanol to obtain 0.24 g of 1-amino-2,3-dihydro-4,6-dimethyl-7-hydroxy-2-phenyl-1H-indene Colorless needlelike crystals. Melting point: 135°-136° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05242919
出典データセットuspto-grants-1993_09
ORD IDord-484afa8140964d98ab10e3c32c381780
出典メモuspto-grants-1993_09