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HRID 414693作成日:2026年10月25日

Hydrochloric Acid → 1-n-Butylamino-4,6-dimethyl-7-hydroxyindane hydrochloride

https://huagongshe.com/reaction/414693

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物ButylamineHCID 8007—
反応物4,6-Dimethyl-7-hydroxy-1-indanoneHCID 240718—
反応物Sodium AcetateHCID 517045—
反応物Sodium borohydrideHCID 4311764—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物1-n-Butylamino-4,6-dimethyl-7-hydroxyindane hydrochlorideHCID 13604203—

反応手順

100 Milliliters of ethanol solution containing 1.76 g of 4,6-dimethyl-7-hydroxy-1-indanone and 14.6 g of n-butylamine was refluxed by heating for 8 hours. The reaction mixture was cooled to a room temperature, then 1.0 g of sodium borohydride was added thereto. The mixture was further stirred at a room temperature for 1 hour. The reaction mixture was concentrated to dryness and the residue obtained was dissolved in 100 ml of water. Then the solution was acidified by adding a concentrated hydrochloric acid, and the pH of the solution was adjusted to about pH=9 by adding a saturated sodium acetate aqueous solution. The precipitate formed was extracted with ethyl acetate, washed with water and dried. The solvent was removed by evaporation, the residue obtained was dissolved in 100 ml of ethanol, and changed to hydrochloride by adding ethanol being saturated with hydrogen chloride gas. Recrystallized from ethanol-ether to obtain 1.89 g of 1-n-butylamino-4,6-dimethyl-7-hydroxyindane hydrochloride in the form of colorless needle-liee crystals. Melting point: 143°-144° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04792628
出典データセットuspto-grants-1988_12
ORD IDord-a57bc510ba94475d92c3cf9b77a8736b
出典メモuspto-grants-1988_12