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HRID 257044作成日:2026年10月25日

Triethylamine → N-ethoxycarbonyl-m-bromophenethylamine

https://huagongshe.com/reaction/257044

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ethyl chloroformateHCID 10928—
反応物3-BromophenethylamineHCID 7021736—
溶媒DichloromethaneHCID 6344—
生成物N-ethoxycarbonyl-m-bromophenethylamineHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05260316
出典データセットuspto-grants-1993_11
ORD IDord-ee8701aded72479ca304cde5cd352229
出典メモuspto-grants-1993_11