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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2258416Generated: November 1, 2026

Ethylthiol trifluoroacetate → Deoxyuridine

https://huagongshe.com/reaction/2258416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylthiol trifluoroacetateHCID 67844—
Reactant2'-Amino-2'-deoxyuridineHCID 6482479—
SolventMethanolHCID 887—
ProductDeoxyuridineHCID 13712—

Reaction Steps

To a suspension of 2'-amino,2'-deoxyuridine (2.0 g, 8.22 mmoles) in methanol (150 ml) was added S-ethyl trifluorothioacetate (1.6 ml, 12.48 mmoles, 1.5 eq.). This mixture was stirred at room temperature overnight. Nitrogen was bubbled through the reaction mixture for 2 h to remove volatile thio-byproducts. The mixture was evaporated to dryness and the solid was recrystallized from methanol/chloroform to yield 2.3 g (82%) of 2'-trifluoroacetylamino, 2'-deoxyuridine. The analytical data agreed with the literature (Imazawa and Eckstein (1979) supra).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05660985
Source datasetuspto-grants-1997_08
ORD IDord-fd6c4cb344a24c5e9a81abadae4fd274
Source noteuspto-grants-1997_08