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HRID 2300162作成日:2026年10月27日

Tert-butyl 4-(2-(benzyloxy)-3-(tert-butoxy)propyl]-4-hydroxy-1-piperidinecarboxylate → Tert-butyl 4-[2-(benzyloxy)-3-hydroxypropyl]-4-hydroxy-1-piperidinecarboxylate

https://huagongshe.com/reaction/2300162

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-butyl 4-(2-(benzyloxy)-3-(tert-butoxy)propyl]-4-hydroxy-1-piperidinecarboxylateHCID 22744588—
反応物Ammonium cerium-nitrateHCID 57418452—
溶媒AcetonitrileHCID 6342—
生成物Tert-butyl 4-[2-(benzyloxy)-3-hydroxypropyl]-4-hydroxy-1-piperidinecarboxylateHCID 2274464826.7%

反応手順

2.36 g of tert-butyl 4-[2-(benzyloxy)-3-(tert-butoxy)propyl]-4-hydroxy-1-piperidinecarboxylate was dissolved in 40 ml acetonitrile, 426 mg of cerium ammonium nitrate was added thereto, and the mixture was stirred at room temperature overnight. Silica gel was added to the reaction solution, and then it was evaporated. It was purified by adsorptive silica gel charged in a non-adsorptive silica gel column with hexane-ethyl acetate to give 547 mg of tert-butyl 4-[2-(benzyloxy)-3-hydroxypropyl]-4-hydroxy-1-piperidinecarboxylate.

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-8d22fd94ad45462797cbfecb71441228
出典メモuspto-grants-2002_12