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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 414693생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/414693

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물ButylamineHCID 8007—
반응물4,6-Dimethyl-7-hydroxy-1-indanoneHCID 240718—
반응물Sodium AcetateHCID 517045—
반응물Sodium borohydrideHCID 4311764—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물1-n-Butylamino-4,6-dimethyl-7-hydroxyindane hydrochlorideHCID 13604203—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04792628
출처 데이터셋uspto-grants-1988_12
ORD IDord-a57bc510ba94475d92c3cf9b77a8736b
출처 메모uspto-grants-1988_12