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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234974Generated: October 30, 2026

Pyridine → HCID 67717591, compound

https://huagongshe.com/reaction/234974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 22853714HCID 22853714—
Reactant5'-(t-Butyldimethylsilyl)-5-methyl-3'-deoxy-uridineHCID 53759132—
Catalystchromium (VI) trioxideHCID 10219390—
CatalystHCID 131712986HCID 131712986—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 67717591HCID 6771759159.6%

Reaction Steps

Chromium trioxide (7.63 g, 76.3 mmol) was added to 150 mL of dry methylene chloride containing 12.059 g (152.6 mmol) of pyridine. The mixture was stirred for 15 minutes. In a separate flask, 793 mg (19.08 mmol) of 5'-O-(t-butyldimethylsilyl)-5-methyl-3'-deoxyuridine from Step 2 was dissolved in approximately 100 mL of methylene chloride. The chromium trioxide-pyridine solution was added to the solution of 5'-(t-butyldimethylsilyl)-5-methyl-3'-deoxy-uridine and 1.946 g (19.08 mmol) of acetic anhydride was added immediately. After stirring at ambient temperature for 0.5 h, the reaction mixture was diluted with approximately 250 mL of ethyl acetate then filtered through Celite filter aid and through florisil eluted with ethyl acetate. The solvent was evaporated and the residue purified on silica gel eluted with 90% ethyl acetate in hexanes. The title compound was obtained in 59.6% yield (4.08 g), [α]D23 =+38.0° (c, 1.31, MeOH). Analysis calculated for C16H26N2O5Si: C, 54.29; H, 7.34; N, 7.91. Found: C, 54.25; H, 7.36; N, 7.88

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597824
Source datasetuspto-grants-1997_01
ORD IDord-e41f20adc3334292a328f82f4374f460
Source noteuspto-grants-1997_01