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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22516생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/22516

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참여 물질

역할이름HCID투입량
반응물1-Bromo-2-ChloroethaneHCID 7849—
반응물2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
반응물1-(Carboethoxy)-1-(4-methoxybenzylthio)methaneHCID 10847644—
반응물Lithium bis(trimethylsilyl)amideHCID 57426343—
용매TetrahydrofuranHCID 8028—
생성물1-(Carboethoxy)-1-(4-methoxybenzylthio)cyclopropaneHCID 2240021721%

반응 조건

온도-78 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428158
출처 데이터셋uspto-grants-1995_06
ORD IDord-dab25ad53b5e47e6a2206dae9c9bc9f1
출처 메모uspto-grants-1995_06