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HRID 471048作成日:2026年10月27日
Ethyl bromodifluoroacetate → tert-Butyl 4-((2-bromo-2,2-difluoroacetamido)methyl)-4-hydroxypiperidine-1-carboxylate
https://huagongshe.com/reaction/471048
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl bromodifluoroacetate | HCID 69585 | — |
| 反応物 | tert-Butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate | HCID 23396319 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | tert-Butyl 4-((2-bromo-2,2-difluoroacetamido)methyl)-4-hydroxypiperidine-1-carboxylate | HCID 57988980 | — |
反応手順
A solution of tert-butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate (1.702 g) in DMF (20 mL) at 20° C. was treated with ethyl 2-bromo-2,2-difluoroacetate (1.5 g) and the mixture stirred for 90 minutes at 20° C. under nitrogen. The mixture was partitioned between ethyl acetate and brine, the organic layer was washed twice with brine, dried over sodium sulphate, filtered and the solvent evaporated under reduced pressure to afford the subtitled compound. Yield 2.5 g.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08629271B2 |
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| 出典データセット | uspto-grants-2014_01 |
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| ORD ID | ord-435b4c8bbeae44fe81601b8d05ad124c |
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| 出典メモ | uspto-grants-2014_01 |
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