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HRID 47326作成日:2026年10月26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/47326

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US06699870B2
出典データセットuspto-grants-2004_03
ORD IDord-da61023537e6496ab9c1190c0d24d14d
出典メモuspto-grants-2004_03