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HRID 2201685作成日:2026年10月25日

Ethyl chloroformate → Tert-butyl ethyl (4-(thiophen-2-yl)-1,2-phenylene)dicarbamate

https://huagongshe.com/reaction/2201685

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl chloroformateHCID 10928—
反応物tert-Butyl (2-amino-4-(thiophen-2-yl)phenyl)carbamateHCID 57717474—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Tert-butyl ethyl (4-(thiophen-2-yl)-1,2-phenylene)dicarbamateHCID 7100730944%

反応手順

To a solution of tert-butyl (2-amino-4-(thiophen-2-yl)phenyl)carbamate (0.20 g, 0.69 mmol, 1.0 equiv.) in dichloromethane (4 mL) was added ethyl chloroformate (0.08 mL, 0.83 mmol, 1.2 equiv.), TEA (0.19 mL, 1.37 mmol, 2.0 equiv.) and DMAP (8 mg, 0.07 mmol, 0.1 equiv.) at 0° C. The reaction was warmed to room temperature and stirred for 16 h. The reaction was then diluted with dichloromethane and water. The organic layer was separated, washed with water and brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude material was purified on column chromatography (silica gel, 20% EtOAc/hexanes) to give tert-butyl ethyl (4-(thiophen-2-yl)-1,2-phenylene)dicarbamate (0.11 g, 44% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09365498B2
出典データセットuspto-grants-2016_06
ORD IDord-db55e1f2f4cb4fb69d87d452b8104580
出典メモuspto-grants-2016_06