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HRID 1021426作成日:2026年10月25日

Oxalyl chloride → Ethyl 6,8-dichloro-7-(4-(4-chlorophenethylcarbamoyl)phenoxy)chroman-4-carboxylate

https://huagongshe.com/reaction/1021426

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalyl chlorideHCID 65578—
反応物2-(4-Chlorophenyl)ethylamineHCID 67430—
反応物DiisopropylethylamineHCID 81531—
反応物4-(6,8-Dichloro-4-(ethoxycarbonyl)chroman-7-yloxy)benzoic acidHCID 67080303—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 6,8-dichloro-7-(4-(4-chlorophenethylcarbamoyl)phenoxy)chroman-4-carboxylateHCID 6708046198.2%

反応手順

4-(6,8-Dichloro-4-(ethoxycarbonyl)chroman-7-yloxy)benzoic acid (22.96 g, 55.832 mmol) was dissolved in dichloromethane (200 ml) and DMF (0.2 ml). Oxalyl chloride (8.6 ml, 98.585 mmol) was added slowly over a period of 30 minutes at ambient temperature. The crude mixture was concentrated under reduced pressure. Dry dichloromethane (200 ml) was added and the mixture was cooled in an ice bath. 2-(4-Chlorophenyl)ethylamine (8.5413 ml, 61.415 mmol) and diisopropylethylamine (11.701 ml, 66.999 mmol) were added sequentially to the mixture. The mixture was stirred in an ice bath for 10 minutes and warmed to ambient temperature. The crude mixture was washed with 1N HCl (100 ml), water (2×50 ml), and brine (50 ml), dried over MgSO4, filtered through GF paper, and concentrated to provide 30.1 g of a light brown solid after drying under high vacuum for 2 hours. The crude solid was recrystallized from hot EtOAc-hexanes to provide 26.8 g of the title compound as a light brown solid (87%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08716498B2
出典データセットuspto-grants-2014_05
ORD IDord-98af8070bc95400482aabdac6d169202
出典メモuspto-grants-2014_05