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HRID 39683作成日:2026年10月25日

Methanol → 1-[(2-Bromoethyl)sulfanyl]-3-fluorobenzene

https://huagongshe.com/reaction/39683

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物1,2-DibromoethaneHCID 7839—
反応物m-FluorobenzenethiolHCID 75710—
反応物Sodium methanolate methanolHCID 23694274—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物1-[(2-Bromoethyl)sulfanyl]-3-fluorobenzeneHCID 22470626—

反応手順

To 2 mL of a methanol solution containing 0.83 g of 28% sodium methoxide/methanol, 1.0 mL of 1,2-dibromoethane and 0.50 g of 3-fluorobenzenethiol were added under cooling with ice, the mixture was stirred at the same temperature for 1 hour, at room temperature for 2 hours, and at 50° C. for 1 hour, and then the reaction mixture was refluxed by heating for 5 hours. The reaction mixture was cooled to room temperature, and then ethyl acetate and water were added thereto. The organic layer was separated, washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent; hexane] to obtain 0.62 g of a pale yellow oily substance, 1-(3-fluorophenyl)thio-2-bromoethane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524738B2
出典データセットuspto-grants-2013_09
ORD IDord-4c599ba040dc492a8ebc1ad9adb1f598
出典メモuspto-grants-2013_09