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HRID 2300164作成日:2026年10月25日

Tert-butyl 3-(benzyloxy)-1-oxa-8-azaspiro[4.5]decane-8-carboxylate → tert-Butyl 3-hydroxy-1-oxa-8-azaspiro[4.5]decane-8-carboxylate

https://huagongshe.com/reaction/2300164

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-butyl 3-(benzyloxy)-1-oxa-8-azaspiro[4.5]decane-8-carboxylateHCID 22744533—
反応物HCID 178418361HCID 178418361—
触媒HCID 178418390HCID 178418390—
溶媒TetrahydrofuranHCID 8028—
生成物tert-Butyl 3-hydroxy-1-oxa-8-azaspiro[4.5]decane-8-carboxylateHCID 2274454989.1%

反応手順

6.47 g of tert-butyl 3-(benzyloxy)-1-oxa-8-azaspiro[4.5]decane-8-carboxylate was dissolved in 100 ml tetrahydrofuran, 1.3 g palladium carbon was added thereto, and the mixture was stirred overnight in a hydrogen atmosphere. The catalyst was filtered off from the reaction solution, 1.3 g of palladium carbon was added thereto, and the solution was stirred overnight in a hydrogen atmosphere. The catalyst was filtered off from the reaction solution, 2.6 g of palladium carbon was added thereto, and the solution was stirred overnight in a hydrogen atmosphere at 4.2 atmospheric pressure. The catalyst was filtered off from the reaction solution, the solvent was evaporated, and the resulting residue was purified by silica gel column chromatography (ethyl acetate/methanol) to give 4.27 g of tert-butyl 3-hydroxy-1-oxa-8-azaspiro[4.5]decane-8-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06498159B1
出典データセットuspto-grants-2002_12
ORD IDord-9568fe80ede14ae1be604142cfec6a1f
出典メモuspto-grants-2002_12