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HRID 22516作成日:2026年10月26日

1-Bromo-2-Chloroethane → 1-(Carboethoxy)-1-(4-methoxybenzylthio)cyclopropane

https://huagongshe.com/reaction/22516

反応式

関与物質

役割名称HCID仕込み量
反応物1-Bromo-2-ChloroethaneHCID 7849—
反応物2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
反応物1-(Carboethoxy)-1-(4-methoxybenzylthio)methaneHCID 10847644—
反応物Lithium bis(trimethylsilyl)amideHCID 57426343—
溶媒TetrahydrofuranHCID 8028—
生成物1-(Carboethoxy)-1-(4-methoxybenzylthio)cyclopropaneHCID 2240021721%

反応条件

温度-78 °C

反応手順

Cool lithium hexamethyldisilazane (6 mL of a 1.0M solution in tetrahydrofuran, 6.0 mmol) to -78° C. Add, by cannula transfer, a solution of 1-(carboethoxy)-1-(4-methoxybenzylthio)methane (1.36 g, 5.66 mmol) in tetrahydrofuran (10 mL). Stir for 45 minutes, add 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone (DMPU) (0.73 mL, 6.0 mmol) followed by 1-bromo-2-chloroethane (050 mL, 6.0 mmol) and stir to room temperature overnight. Cool to -78° C., add lithium hexamethyldisilazane (6.0 mL, 6.0 mmol) and stir at room temperature for 24 hours. Quench with saturated ammonium chloride (5 mL) and partition between ethyl acetate (30 mL) and water (30 mL). Separate the organic phase, dry (Na2SO4) and evaporate the solvent in vacuo. Purify by chromatography (5:1 hexane/ethyl acetate to 2.5:1 hexane/ethyl acetate) to give 1-(carboethoxy)-1-(4-methoxybenzylthio)cyclopropane (317 mg, 21%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428158
出典データセットuspto-grants-1995_06
ORD IDord-dab25ad53b5e47e6a2206dae9c9bc9f1
出典メモuspto-grants-1995_06