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Trimethylsilyldiazomethane → Methyl 1-(3-bromo-5-cyanophenyl)piperidine-4-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Trimethylsilyldiazomethane | HCID 167693 | — |
| 反応物 | 1-(3-Bromo-5-cyanophenyl)piperidine-4-carboxylic acid | HCID 59588189 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | Methyl 1-(3-bromo-5-cyanophenyl)piperidine-4-carboxylate | HCID 59588037 | 100% |
反応手順
To a solution of 1-(3-bromo-5-cyanophenyl)piperidine-4-carboxylic acid (1.1 g, 3.6 mmol) in toluene (4 mL) and methanol (2 mL) was added TMSCHN2 (2 M in Et2O, 3.5 mL, 7.0 mmol) dropwise at room temperature. After 1 h, the reaction was quenched with acetic acid (˜0.1 mL), diluted with EtOAc and washed with saturated aqueous NaHCO3. The organic layer was separated, dried (MgSO4), and concentrated to give methyl 1-(3-bromo-5-cyanophenyl)piperidine-4-carboxylate in ˜100% yield.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08530480B2 |
| 出典データセット | uspto-grants-2013_09 |
| ORD ID | ord-852a98529a0f4ee78c517dafdbe85afc |
| 出典メモ | uspto-grants-2013_09 |