Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248285Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 86746820, compound

https://huagongshe.com/reaction/248285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 86746821HCID 86746821—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86746820HCID 86746820—

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"-propyloxycyclohexyl)-1'-methylvinyl]-14-triisopropylsiloxy-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9 ]octacos18-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 temperature is raised to room temperature, reaction was poured into water, and extracted with ethyl acetate (three times). Combined organic layers were 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 numberUS05208228
Source datasetuspto-grants-1993_05
ORD IDord-b7f6a749c31c45fabff5ab6323907746
Source noteuspto-grants-1993_05