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HRID 35599作成日:2026年10月25日

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

https://huagongshe.com/reaction/35599

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WaterHCID 962—
反応物(3-Methoxyphenyl)acetonitrileHCID 88310—
反応物(Dimethyl sulfide)trihydroboronHCID 12423031—
溶媒EthanolHCID 702—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物Benzeneethanamine, 3-methoxy-, hydrochloride (1:1)HCID 197751—

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04767769
出典データセットuspto-grants-1988_08
ORD IDord-ad7091e54e4d4f1c95e189f5baa43431
出典メモuspto-grants-1988_08