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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645302Generated: October 25, 2026

Dimethyl Sulfoxide → Acetic Acid 4-(tert-butyl-diphenyl-silanyloxy)-2-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-5-formyl-tetrahydro-furan-3-yl Ester

https://huagongshe.com/reaction/1645302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantTrichloroacetic anhydrideHCID 20079—
ReactantAcetic Acid 4-(tert-butyl-diphenyl-silanyloxy)-2-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-5-hydroxymethyl-tetrahydro-furan-3-yl EsterHCID 66774584—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductAcetic Acid 4-(tert-butyl-diphenyl-silanyloxy)-2-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-5-formyl-tetrahydro-furan-3-yl EsterHCID 86594161—

Reaction Steps

To a mixture of trichloroacetic anhydride (1.5 eq.) and dimethylsulfoxide (2.0 eq.) in dichloromethane at −78° C. is added a solution of Compound 9 in dichloromethane. After 30 minutes, triethylamine (4.5 eq.) is added. Subsequently, the mixture is poured into ethyl acetate, washed with water and brine, dried over anhydrous sodium sulfate, and evaporated to dryness. The resulting material is carried into the next step without further purification. This procedure has been used to prepare the related 4′-C-α-formyl nucleosides (Nomura, M., et. al., J. Med. Chem. 1999, 42, 2901-2908).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124745B2
Source datasetuspto-grants-2012_02
ORD IDord-6e61b3dea8ce4b43b90bee7f87fbe63f
Source noteuspto-grants-2012_02