戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 993193作成日:2026年10月25日

tert-Butanol → Benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate

https://huagongshe.com/reaction/993193

反応式

関与物質

役割名称HCID仕込み量
反応物tert-ButanolHCID 6386—
反応物Benzyl 4-isocyanatopiperidine-1-carboxylateHCID 2776273—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物Benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylateHCID 21981786—

反応手順

A solution of 3.2 g (12.3 mmol) of (1-benzyloxycarbonylpiperidin-4-yl)isocyanate from Step A in 25 mL of DMF was slowly added to a suspension of CuCl3 in 25 mL of DMF and 12 mL of t-butanol. The reaction was stirred for 24 h and then diluted with water and extracted twice with 1:1 ether: ethyl acetate. The organic layers were each washed with a portion of water and brine, dried over sodium sulfate, combined and concentrated. The residue was purified by FC eluting with 20% ethyl acetate in hexanes to afford 685 mg of title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06472410B1
出典データセットuspto-grants-2002_10
ORD IDord-c69a86db3f494bc6af5f4ea6a6877d96
出典メモuspto-grants-2002_10