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HRID 279161作成日:2026年10月26日

3,5-Dinitrobenzoic acid → HCID 86749722、化合物

https://huagongshe.com/reaction/279161

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-Dinitrobenzoic acidHCID 7433—
反応物Diisopropyl EtherHCID 7914—
反応物TriphenylphosphineHCID 11776—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物HCID 86749723HCID 86749723—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 86749722HCID 86749722—

反応手順

2-(2-Fluorophenyl)-2-[(l1R)-1-(3,4,5,6-tetrahydro-2H-pyran-2-yl)oxyethyl] oxirane (synthesized by the method described in EP0548553A) was converted into (1R)-1-[2-(2-fluorophenyl)-2-oxiranyl]ethanol by the method described in Reference Example 1. To an ice-cooled solution of this compound (34.77 g) in tetrahydrofuran (600 ml) were added triphenylphosphine (127.21 g), 3,5-dinitrobenzoic acid (102.88 g) and diethyl azodicarboxylate (84.47 g). The mixture was stirred at room temperature for 7 hours under an argon atmosphere, and then ethyl acetate (600 ml), diisopropyl ether (100 ml) and water (800 ml) were added. The separated aqueous layer was extracted with ethyl acetate (600 ml, 400 ml). The organic layers were combined, washed with water and a saturated aqueous solution of sodium chloride successively, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel chromatography (eluent: hexane/ethyl acetate=5/1) and recrystallized from ethyl acetate to give [(1S)-1-[(2R)-2-(2-fluorophenyl)-2-oxiranyl]ethyl] 3,5-dinitrobenzoate (23.15 g) as colorless needles.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06362206B1
出典データセットuspto-grants-2002_03
ORD IDord-04f57a965b214a38bbfbe8ba3893900b
出典メモuspto-grants-2002_03