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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395841Generated: October 30, 2026

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

https://huagongshe.com/reaction/2395841

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 numberUS05489677
Source datasetuspto-grants-1996_02
ORD IDord-6a0b67bb9a6a4b159dc3e8da0f70a78a
Source noteuspto-grants-1996_02