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HRID 272792作成日:2026年10月27日

1-Benzylpiperidin-4-ol → 1-benzyl-4-piperidyl N-(2-biphenylyl)carbamate

https://huagongshe.com/reaction/272792

反応式

関与物質

役割名称HCID仕込み量
反応物1-Benzylpiperidin-4-olHCID 78461—
反応物1-Isocyanato-2-phenylbenzeneHCID 222280—
溶媒AcetonitrileHCID 6342—
生成物1-benzyl-4-piperidyl N-(2-biphenylyl)carbamateHCID 10500369—

反応条件

温度85 °C

反応手順

In a 50 ml sealed tube was added 2-biphenylylisocyanate (8 g, 41 mmol) in anhydrous acetonitrile (40 mL). To this solution was added N-benzyl-4-piperidinol (9.8 g, 51.25 mmol) and the tube was partially immersed in a silicon oil bath and heated to 85° C. After 16 h, the reaction mixture was cooled and concentrated in vacuo to give a 1-benzyl-4-piperidyl N-(2-biphenylyl)carbamate which was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07456203B2
出典データセットuspto-grants-2008_11
ORD IDord-dfba0cfa044b47189426397db92aff74
出典メモuspto-grants-2008_11