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HRID 345497作成日:2026年10月26日

Hydrochloric Acid → 1-(4-Methoxy-5,6,7,8-tetrahydro-1-naphthyl)-2-ethyl-3-pyrrolidino-1-propanone

https://huagongshe.com/reaction/345497

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FormaldehydeHCID 712—
反応物Pyrrolidine, hydrochloride (1:1)HCID 212848—
反応物1-(4-Methoxy-5,6,7,8-tetrahydro-1-naphthyl)-1-butanoneHCID 14994236—
溶媒IsopropanolHCID 3776—
生成物1-(4-Methoxy-5,6,7,8-tetrahydro-1-naphthyl)-2-ethyl-3-pyrrolidino-1-propanoneHCID 1407133462.8%

反応手順

A mixture of 1-(4-methoxy-5,6,7,8-tetrahydro-1-naphthyl)-1-butanone (2.50g), paraformaldehyde (0.42g), pyrrolidine hydrochloride (1.51g), and hydrochloric acid (0.2 ml) in isopropyl alcohol (7 ml) was refluxed for 15 hrs. The reaction mixture was evaporated in vacuo to give the residue. The residue was partitioned into water and ethyl ether. The aqueous layer, was extracted, neutralized with ammonia water, and then extracted with ethyl ether. The organic layer was dried over anhydrous magnesium sulfate. The mixture was filtered and the filtrate was evaporated in vacuo to give 1-(4-methoxy-5,6,7,8-tetrahydro-1-naphthyl)-2-ethyl-3-pyrrolidino-1-propanone (2.13 g, Yield: 62.8 %) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05057535
出典データセットuspto-grants-1991_10
ORD IDord-c8f0fe61614e40adb00ef055c2d4b977
出典メモuspto-grants-1991_10