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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492008Generated: October 29, 2026

Dimethyl Sulfoxide → HCID 57166164, compound

https://huagongshe.com/reaction/1492008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86748309HCID 86748309—
SolventDichloromethaneHCID 6344—
ProductHCID 57166164HCID 57166164—

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a solution of 0.48 g (0.00383 mole) of oxalyl chloride in 7 ml of methylene chloride is added dropwise a solution of 0.54 g (0.0067 mole) of dimethylsulfoxide in 4 ml of dichloromethane with stirring at -60° C. After stirring the mixture for another 10 min at -70° C., a solution of 0.95 g (0.00244 mole) of (2S,3S,4R)-4-(biphenyl)-4-ylmethoxy)-3-(3-hydroxyprop-1-yl)-2-(3-pyridyl)tetrahydrofuran in 8 ml of dichloromethane is added dropwise over a period of 10 min. The mixture is stirred at -70° C. for 1 h and 2.48 ml (0.014 mole) of diisopropylethyl amine are added at once. The mixture is allowed to warm up to room temperature, washed with water and brine, dried (MgSO4) and evaporated. The residue is purified by flash chromatography using methylene chloride-methanol-ammonium hydroxide (300:25:1) as eluent to give (2S,3S,4R)-3-[4-(biphenyl-4-ylmethoxy)-2-(3-pyridyl)tetrahydrofuran-3-yl]propanal as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05371096
Source datasetuspto-grants-1994_12
ORD IDord-70b0d3f12d64470eb1a457b42d971cfd
Source noteuspto-grants-1994_12