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HRID 129113作成日:2026年10月23日

3,5-Dinitrobenzoyl chloride → [(1R)-1-[(2R)-2-(2,4-Difluorophenyl)-2-oxiranyl]ethyl]3,5-dinitrobenzoate

https://huagongshe.com/ja/reaction/129113

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-Dinitrobenzoyl chlorideHCID 7432—
反応物(1R)-1-[2-(2,4-difluorophenyl)-2-oxiranyl]ethanolHCID 15130436—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物[(1R)-1-[(2R)-2-(2,4-Difluorophenyl)-2-oxiranyl]ethyl]3,5-dinitrobenzoateHCID 1069199846.3%

反応手順

(1R)-1-[2-(2,4-Difluorophenyl)-2-oxiranyl]ethanol (31.5 g) and 40 g of 3,5-dinitrobenzoyl chloride were dissolved in 500 ml of methylene chloride and, with ice cooling, 24.1 ml of triethylamine was added dropwise thereinto. The reaction solution was stirred at room temperature for 3.5 hours, washed with 150 ml of water and then with 150 ml of 5% aqueous solution of sodium bicarbonate, dried over magnesium sulfate and concentrated under reduced pressure. The crystals separated out were collected by filtration and washed with methylene chloride. The mother liquor and the washing were combined and distilled off under reduced pressure, then 25 ml of ethyl acetate and 300 ml of methanol were added to the residue and the mixture was cooled with ice. The crystals separated out were collected by filtration and recrystallized from a mixture of 25 ml of ethyl acetate and 250 ml of methanol to give 28.7 g of [(1R)-1-[(2R)-2-(2,4-difluorophenyl)- 2-oxiranyl]ethyl]3,5-dinitrobenzoate as colorless needles.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05466820
出典データセットuspto-grants-1995_11
ORD IDord-9f3b944ca2bf4daebaf0cfcbaf2973f1
出典メモuspto-grants-1995_11