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HRID 19464作成日:2026年10月26日

tert-Butyl ((1-benzylpiperidin-4-yl)methyl)carbamate → Tert-butyl (piperidin-4-ylmethyl)carbamate

https://huagongshe.com/reaction/19464

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl ((1-benzylpiperidin-4-yl)methyl)carbamateHCID 2824066—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物Tert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429100%

反応手順

A solution of 1-benzyl-4-tertbutyloxycarbonylaminomethylpiperidine 8 (4.79 g; 15.7 mmol) in 120 ml of MeOH is poured into a hydrogenation reactor. The 10% Pd/C-based catalyst is added (0.872 g; 0.82 mmol) and the mixture is subjected to a hydrogen pressure of 3.5 bars (50 psi) for 24 hours in a Parr type shaker. After filtration on celite and washing with methanol, the medium is concentrated in order to produce 3.36 g (Yield=100%) of product in the form of white crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745413B2
出典データセットuspto-grants-2010_06
ORD IDord-389f564054af4404af46e958b7bcb7da
出典メモuspto-grants-2010_06