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HRID 2283262作成日:2026年10月25日

Diethyl chlorophosphate → 1-Bromo-4-[(E)-2-ethoxysulfonylethenyl]benzene

https://huagongshe.com/reaction/2283262

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl chlorophosphateHCID 13139—
反応物4-BromobenzaldehydeHCID 70741—
反応物1-PropanesulfonateHCID 4431756—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物1-Bromo-4-[(E)-2-ethoxysulfonylethenyl]benzeneHCID 8663200264%

反応条件

温度0 °C

反応手順

n-Butyllithium (59.0 mL, 1.6M solution in hexanes) was added dropwise during 25 min to a solution of ethylmethanesulfonate (9.1 mL, 86 mmol) in THF (200 mL) at −78° C. The reaction mixture was stirred for 15 min then diethyl chlorophosphate (7.2 ml, 50 mmol) was added dropwise. The solution was stirred at −78° C. for 30 min, allowed to warm to 0° C. and then cooled to −78° C. again. 4-Bromobenzaldehyde (9.2 g, 50 mmol) in THF (50 mL) was then added dropwise during 15 minutes and the resulting mixture was then allowed to slowly reach RT and stirred overnight. Water (20 mL) was added to the mixture and the reaction was concentrated in vacuo. The residue was extracted with diethyl ether and the combined organic extracts were washed with aqueous saturated sodium chloride, dried over magnesium sulfate, filtered and the solvent was evaporated in vacuo. Purification by column chromatography, using 15% ethyl acetate/hexanes as the eluent, afforded the title compound (9.3 g, 64%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09145380B2
出典データセットuspto-grants-2015_09
ORD IDord-e6e13d12bb50468b8e062189a5b6d9dd
出典メモuspto-grants-2015_09