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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375553Generated: October 25, 2026

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

https://huagongshe.com/reaction/375553

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-ChloroethaneHCID 7849—
Reactant2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
Reactant1-(Carboethoxy)-1-(4-methoxybenzylthio)methaneHCID 10847644—
ReactantLithium bis(trimethylsilyl)amideHCID 57426343—
SolventTetrahydrofuranHCID 8028—
Product1-(Carboethoxy)-1-(4-methoxybenzylthio)cyclopropaneHCID 2240021721%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Cool lithium hexamethyldisilazane (6 mL of a 1.0M solution 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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05486513
Source datasetuspto-grants-1996_01
ORD IDord-6fa1becc54914fbeb8ef2d6422006083
Source noteuspto-grants-1996_01