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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633829Generated: October 31, 2026

Dimethyl Sulfoxide → HCID 86758781, compound

https://huagongshe.com/reaction/1633829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 86758780HCID 86758780—
SolventDichloromethaneHCID 6344—
ProductHCID 86758781HCID 8675878191.1%

Reaction Steps

To a solution of oxalyl chloride (0.21 mL, 2.4 mmol) in anhydrous dichloromethane (30 mL) at −78° C. under nitrogen atmosphere, dimethylsulfoxide (0.36 mL, 5.0 mmol) was added and stirred for 30 minutes. To this mixture, a solution of ethyl (1SR,2SR,3RS)-2-hydroxymethyl-3-ethylcyclopropane carboxylate (350 mg, 2.0 mmol) in anhydrous dichloromethane (20 mL) was added and reaction stirred at the same temperature for 45 minutes. Then, triethylamine (1.4 mL, 10.0 mmol) was added and the mixture was allowed to react at room temperature. After 30 minutes, the reaction was quenched with water (30 mL), the layers were separated and the aqueous one was extracted with dichloromethane (2×50 mL). The combined organic layers were dried over sodium anhydride, filtered and evaporated to dryness. The resulting residue was purified by column chromatography using ethyl acetate and hexane 1:4 as eluent to afford 310 mg (90% yield) of ethyl (1SR,2SR,3RS)-2-formyl-3-ethylcyclopropane carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06504052B1
Source datasetuspto-grants-2003_01
ORD IDord-129306cfcf034d6386fbbd88eff092fb
Source noteuspto-grants-2003_01