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HRID 1975539생성일: 2026년 10월 24일

Hydrochloric Acid → 2-(3,5-Dimethyl-phenoxy)-1-methyl-ethylamine

https://huagongshe.com/ko/reaction/1975539

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium IodideHCID 5238—
반응물Ammonium HydroxideHCID 14923—
반응물1-(3,5-Dimethylphenoxy)-2-chloropropaneHCID 19100307—
용매EthanolHCID 702—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물2-(3,5-Dimethyl-phenoxy)-1-methyl-ethylamineHCID 530525783.7%

반응 조건

온도130 °C

반응 단계

A 100 ml autoclave was charged with 1.96 g (9.8 mmol) of 1-(3,5-dimethylphenoxy)-2-chloropropane, 10 ml of ethanol and 0.2 g of sodium iodide, and then 40 ml of a 28% ammonia aqueous solution was added. The mixture was continuously stirred at 130° C. for 8 hours to complete the reaction. After allowed to cool, the reaction mixture was transferred into a 500 ml beaker with 50 ml of water and 20 ml of diethyl ether. A 20% hydrochloric acid aqueous solution was added to the reaction mixture until it became acidic, and the mixture was washed with 20 ml of diethyl ether three times. While the water layer was cooled, a 20% sodium hydroxide aqueous solution was added to make it alkaline, and the water layer was subjected to extraction with 50 ml of diethyl ether three times, and dried over 10 g of anhydrous sodium sulfate. Then, the solvent was distilled off under reduced pressure to give 1.48 g of 1-(3,5-dimethylphenoxy)-2-aminopropane (yield 83.7%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05286905
출처 데이터셋uspto-grants-1994_02
ORD IDord-36a4dc3bc9f2489da306b91df0987b8e
출처 메모uspto-grants-1994_02