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HRID 268517作成日:2026年10月27日

Tilorone Hydrochloride → 2,7-Bis(2-diethylaminoethoxy)fluoren-9-ol dihydrochloride

https://huagongshe.com/reaction/268517

反応式

関与物質

役割名称HCID仕込み量
反応物Tilorone HydrochlorideHCID 33958—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
生成物2,7-Bis(2-diethylaminoethoxy)fluoren-9-ol dihydrochlorideHCID 21552321—

反応条件

温度0 °C

反応手順

A total of 2.3 g (0.06 mole) of sodium borohydride is added in small portions to a stirred solution of 9.7 g (0.02 mole) of 2,7-bis(2-diethylaminoethoxy)fluoren-9-one dihydrochloride in 200 ml or methanol, maintaining the mixture at 0°C throughout the addition. The mixture is allowed to warm to room temperature and the solvent removed in vacuo. The residue is taken up in 10% hydrochloric acid, the mixture extracted with ether, and the aqueous acidic solution evaporated in vacuo. The residue is dissolved in methanol, cooled at -20°C, and the inorganic material which precipitates removed by filtration. The filtrate is evaporated in vacuo, the residue dissolved in water and made basic with 10% aqueous sodium hydroxide. The liberated free base is extracted into ether, the ether extract washed with water and dried over anhydrous magnesium sulfate. The mixture is filtered, the filtrate evaporated, the residue taken up in isopropyl alcohol and acidified to Congo Red with ethereal hydrogen chloride. The precipitated product is collected and recrystallized three times from a mixture of isopropyl alcohol and methanol to give 2,7-bis(2-diethylaminoethoxy)fluoren-9-ol dihydrochloride. M.P. 192°-194°C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03947593
出典データセットuspto-grants-1976_03
ORD IDord-ec0d74681de04e5ab1bec5ae227697bb
出典メモuspto-grants-1976_03