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HRID 2256082作成日:2026年10月27日

1-Boc-6-benzyloctahydropyrrolo[3,4-B]pyridine → 1-Boc-octahydropyrrolo(3,4-b)pyridine

https://huagongshe.com/reaction/2256082

反応式

関与物質

役割名称HCID仕込み量
反応物1-Boc-6-benzyloctahydropyrrolo[3,4-B]pyridineHCID 19029419—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物1-Boc-octahydropyrrolo(3,4-b)pyridineHCID 2256220296.8%

反応手順

In 50 ml of ethanol was dissolved 2.86 g of 6-benzyl-1-t-butoxycarbonyloctahydropyrrolo[3.4-b]pyridine, and 500 mg of 5% palladium-on-carbon was added thereto. While the reaction vessel was heated by a tungsten lamp, hydrogenation was conducted under a pressurized hydrogen gas atmosphere of 4 kg/cm2 for 1.5 hours. After completion of the reaction, the catalyst was removed by filtration, and the filtrate was concentrated to yield 1.98 g of the titled compound as an oily substance.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05654318
出典データセットuspto-grants-1997_08
ORD IDord-10c1ea16223e48f9bee65450198b27ba
出典メモuspto-grants-1997_08