Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232697Generated: October 29, 2026

Dimethyl Sulfoxide → HCID 13854278, compound

https://huagongshe.com/reaction/2232697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 13854277HCID 13854277—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 13854278HCID 1385427872.9%

Reaction Conditions

Temperature-70 °C

Reaction Steps

A solution of dry dimethyl sulphoxide (0.87 g) in dichloromethane (12 cm3) was added dropwise to a stirred solution of oxalyl chloride (0.75 g) in dichloromethane (12 cm3) maintained at -70° C. After a period of five minutes had elapsed, a solution of 2-cyclopropyl-3-(3-phenoxybenzyloxy)propane-1-ol (1.45 g) in dichloromethane (6 cm3) was added dropwise, followed by triethylamine (2.3 g) five minutes later. When the addition was complete the mixture was allowed to warm to the ambient temperature over a period of 2 hours. The reaction mixture was poured into water, and extracted with diethyl ether. The extracts were combined, dried over anhydrous magnesium sulphate and concentrated by evaporation of the solvent. The residual oil (1.5 g) was purified by column chromatography using a silica gel column and eluting with dichloromethane to yield 1-formyl-1-(3-phenoxybenzyloxymethyl)cyclopropane (1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04788348
Source datasetuspto-grants-1988_11
ORD IDord-7ed5d690df994ee796e9b8b9ffa0a7d6
Source noteuspto-grants-1988_11