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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482125Generated: October 29, 2026

Thymidine → 5'-O-tert-Butyldiphenylsilyl-thymidine

https://huagongshe.com/reaction/482125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThymidineHCID 5789—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
Product5'-O-tert-Butyldiphenylsilyl-thymidineHCID 11812846144.7%

Reaction Steps

A mixture of thymidine (400 g, and 1.65 mol), 4-dimethylaminopyridine (0.8 g, 6.5 mmol) and t-butyldiphenylchlorosilane (347.2 g, 1.26 mol) in anhydrous pyridine (3.0 lt) was stirred at room temperature for 48 hr. To the stirred reaction mixture two lots of t-butyldiphenyl chlorosilane (129.4 g, 0.47 mol and 22.7 g, 0.082 mol) were added 12 hr. apart and stirring continued for an additional 48 hr. The reaction mixture was concentrated under vacuum and the residue redissolved in methanol (2.5 lt). The product was precipitated by pouring the reaction mixture into a cold stirred ice-water (5.0 lt) suspension. The aqueous suspension was stirred at room temperature for 3 hr. to quench traces of unreacted chlorosilane. The granular white precipitate was filtered and washed with distilled water (5×1 lt) and air dried to furnish 876 g of 5'-O-t-butyldiphenylsilyl thymidine (slightly contaminated with bissilyated product, about 5%). The impurity was removed by suspending finely powdered 5'-O-t-butyldiphenylsilyl thymidine in ether (600 ml) and pouring into stirred hexanes (1.5 lt).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05792844
Source datasetuspto-grants-1998_08
ORD IDord-3f02dfd9fcce4a40b83648cf17f35c3d
Source noteuspto-grants-1998_08