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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289887Generated: November 2, 2026

Dimethyl Sulfoxide → HCID 123383739, compound

https://huagongshe.com/reaction/1289887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 124026227HCID 124026227—
SolventDichloromethaneHCID 6344—
ProductHCID 123383739HCID 12338373978.9%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of oxalylchloride (0.575 mL, 6.5 mmole) in dichloromethane (10 mL) at -70° C., was added dimethylsulfoxide (0.47 mL, 6.5 mmole). The mixture was stirred at -70° C. for 30 minutes before a solution of Compound (1) (2.4 g, 6.2 mmole) in dichloromethane (18 mL) was added. Stirring at -70° C. was continued for 150 minutes. Triethylamine (4.3 mL, 31 mmole) was added dropwise and the reaction mixture was allowed to warm to room temperature over a 20 hour period. The reaction was quenched by the addition of methanol (2 mL), followed 10 minutes later by 60 mL of water. The phases were separated. The aqueous phase was extracted three times with dichloromethane (60 mL each). The combined organic extracts were washed with solutions of dilute hydrochloric acid followed by saturated sodium bicarbonate and brine. After drying the organic extracts over magnesium sulfate, the solvent was removed under reduced pressure to provide 3'-O-[(dimethyl-1,1-dimethylethyl) silyl]-4'-formyl-thymidine (1.88 g) in crude form as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750343
Source datasetuspto-grants-1998_05
ORD IDord-a63df839da2c46f6abe08a4c474e7dd4
Source noteuspto-grants-1998_05