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HRID 863584作成日:2026年10月26日

Hydrochloric Acid → (2S,3S)-2-phenylpiperidin-3-amine

https://huagongshe.com/reaction/863584

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EthanolHCID 702—
反応物MethanolHCID 887—
反応物CP-99994HCID 5311057—
触媒HCID 178418390HCID 178418390—
溶媒WaterHCID 962—
生成物(2S,3S)-2-phenylpiperidin-3-amineHCID 9812908—

反応手順

In a bottle were placed 9 g of 10% palladium-carbon, 180 ml of methanol, 275 ml of ethanol, 6.5 ml of concentrated hydrochloric acid and 9 g of the hydrochloride salt of (2S,3S)-3-(2-methoxybenzylamino)-2-phenylpiperidine. The mixture was shaken under hydrogen (40 p.s.i.) overnight, after which 9 g of additional catalyst were added to the system and the mixture was shaken under hydrogen for 1 day. The mixture was diluted with water (250 mL), filtered through diatomaceous earth (Celite (trademark)) and the Celite was rinsed well with water. The filtrate was concentrated to a volume of ca. 600-700 mL, made basic with concentrated aqueous sodium hydroxide and extracted with chloroform. The chloroform extracts were dried (sodium sulfate) and concentrated to obtain 4.4 g of the title compound as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05721255
出典データセットuspto-grants-1998_02
ORD IDord-e32cb3f0ef0e44669df25f7b69588d8d
出典メモuspto-grants-1998_02