関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Benzylpiperidin-4-ol | HCID 78461 | — |
| 反応物 | 1-Isocyanato-2-phenylbenzene | HCID 222280 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 1-benzyl-4-piperidyl N-(2-biphenylyl)carbamate | HCID 10500369 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07456203B2 |
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| 出典データセット | uspto-grants-2008_11 |
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| ORD ID | ord-dfba0cfa044b47189426397db92aff74 |
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| 出典メモ | uspto-grants-2008_11 |
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