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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373282Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 57251512, compound

https://huagongshe.com/reaction/373282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 86746333HCID 86746333—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 57251512HCID 57251512—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a cooled solution (-78° C.) of oxalyl chloride added dimethyl sulfoxide dropwise, followed by a solution of 17-ethyl-1-hydroxy-12-[2'-(4"-hydroxy-3"-allyloxycyclohexyl)-1'-methylvinyl]-14-triisopropylsiloxy-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9 ]octacos-18-ene-2,3,10,16-tetraone in dry methylene chloride. The reaction mixture is stirred for 30 min. at -78° C. and then triethylamine is added. The reaction mixture is allowed to rise to room temperature, poured into water, and extracted with ethyl acetate (three times). Combined organic layers are washed (water, sat'd NaHCO3), dried (anhydrous Na2SO4), and filtered. Removal of solvent followed by purification (silica gel column chromatography), gives the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05162334
Source datasetuspto-grants-1992_11
ORD IDord-ffed7bd6a829406cb1626ef10f307a25
Source noteuspto-grants-1992_11