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Trifluoroacetic acid → 2-(4-Benzylpiperidin-1-yl)ethan-1-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Trifluoroacetic acid | HCID 6422 | — |
| 反応物 | [2-(4-Benzyl-piperidin-1-yl)-ethyl]-carbamic acid tert-butyl ester | HCID 59715914 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 2-(4-Benzylpiperidin-1-yl)ethan-1-amine | HCID 2779831 | — |
反応手順
[2-(4-Benzyl-piperidin-1-yl)-ethyl]-carbamic acid tert-butyl ester (1.34 g, 4.2 mmol) is dissolved in CHCl3 (3 mL) and treated with TFA (3 mL) for 2 h at 20° C. The solvent is evaporated, the residue dissolved CH2Cl2 (100 mL) and washed with 1M aqueous NaOH (2×30 mL). The organic layer is dried (Na2SO4), filtered and concentrated to provide the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07375227B2 |
| 出典データセット | uspto-grants-2008_05 |
| ORD ID | ord-613c097532794b6eb35e701bbccad6b1 |
| 出典メモ | uspto-grants-2008_05 |