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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989451Generated: October 29, 2026

Thymidine → HCID 15613767, compound

https://huagongshe.com/reaction/989451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThymidineHCID 5789—
ReactantDichloromethaneHCID 6344—
Reactant9-Fluorenylmethyl chloroformateHCID 34367—
SolventPyridineHCID 1049—
ProductHCID 15613767HCID 1561376776%

Reaction Steps

Thymidine (10 mmol) was dried by coevaporation with dry pyridine (2×30 ml), re-dissolved in dry pyridine (50 ml) and cooled using an acetone/carbon dioxide bath to a temperature of −20° C. The thymidine solution was magnetically stirred and a dichloromethane solution of FMOC-Cl (12 mmol, 1.2 eq. in 20 ml DCM) was added over a period of 60 minutes. The reaction mixture was warmed to room temperature and stirred for additional 60 minutes. The reaction mixture was partitioned between saturated sodium hydrogen carbonate (250 ml) and dichloromethane (3×100 ml). The organic phase was saved, combined, evaporated and dried by coevaporation with toluene (2×50 ml) forming an oily residue. A pure product was crystallized from the oily residue using dichloromethane (30 ml) and benzene (50 ml) as solvent. Yield 76% —white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06639088B2
Source datasetuspto-grants-2003_10
ORD IDord-62b5ae053a7c4400bc949630b969bc78
Source noteuspto-grants-2003_10