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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35599생성일: 2026년 10월 24일

Hydrochloric Acid → Benzeneethanamine, 3-methoxy-, hydrochloride (1:1)

https://huagongshe.com/ko/reaction/35599

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물WaterHCID 962—
반응물(3-Methoxyphenyl)acetonitrileHCID 88310—
반응물(Dimethyl sulfide)trihydroboronHCID 12423031—
용매EthanolHCID 702—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물Benzeneethanamine, 3-methoxy-, hydrochloride (1:1)HCID 197751—

반응 조건

온도0 °C

반응 단계

Borane dimethyl sulphide (45 ml) was added dropwise to a stirred solution of 3-methoxyphenylacetonitrile (32.4 g) in dry tetrahydrofuran (150 ml) under nitrogen. The solution was heated under reflux for 2 hours and was then cooled to 0° C. The solution was stirred under nitrogen at 0° C. as water (74 ml) was added, followed by concentrated hydrochloric acid (149 ml) dropwise over 1 hour. The cloudy solution was heated on a steam bath for 4 hours and then allowed to cool to room temperature. The suspension was diluted with 5N hydrochloric acid (30 ml) and the acidic mixture was washed with ether then basified with 5N sodium hydroxide and extracted with ether. The extracts were washed with water, dried and evaporated to yield a residue which was dissolved in dry ether (50 ml). A saturated solution of hydrogen chloride in ethanol (30 ml) was added followed by more dry ether (150 ml) and the mixture was cooled to 0° C. to yield 2-(3-methoxyphenyl)ethylamine hydrochloride (m.p. 121°-123° C.). The hydrochloride (27.3 g) was dissolved in 5N sodium hydroxide (100 ml) and extracted with ether. The extracts were washed with water (50 ml) and dried. The solvent was removed by evaporation to give the free base.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04767769
출처 데이터셋uspto-grants-1988_08
ORD IDord-ad7091e54e4d4f1c95e189f5baa43431
출처 메모uspto-grants-1988_08