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Triethylamine → N-ethoxycarbonyl-m-bromophenethylamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Ethyl chloroformate | HCID 10928 | — |
| 反応物 | 3-Bromophenethylamine | HCID 7021736 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-ethoxycarbonyl-m-bromophenethylamine | HCID 18963948 | — |
反応手順
A solution of m-bromophenethylamine (6.71 g, 33.55 mmol) and Et3N (7 mL, 50.32 mmoL) in CH2Cl2 (100 mL) is cooled to 0° and ethyl chloroformate (4 mL, 50.32 mmoL) is added. After addition is complete the resulting mixture is allowed to come to room temperature and the solvent is removed in vacuo. The residue is then dissolved in EtOAc (200 mL) and the organic phase washed with 2N HCl (1×250 mL), H2O (1×200 mL), saturated NaHCO3 solution (1×200 mL), saturated NaCl solution (1×200 mL), dried over MgSO4 and concentrated in vacuo to give N-ethoxycarbonyl-m-bromophenethylamine.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05260316 |
| 出典データセット | uspto-grants-1993_11 |
| ORD ID | ord-ee8701aded72479ca304cde5cd352229 |
| 出典メモ | uspto-grants-1993_11 |