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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713375Generated: November 1, 2026

Trityl chloride → 1-(3-Hydroxymethyl-4-trityloxybutyl)-1H-pyrimidine-2,4-dione

https://huagongshe.com/reaction/1713375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
Reactant1-[4-Hydroxy-3-(hydroxymethyl)-1-butyl]-uracilHCID 289650—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-(3-Hydroxymethyl-4-trityloxybutyl)-1H-pyrimidine-2,4-dioneHCID 5946375734%

Reaction Steps

To a solution of compound 35 (45 g, 0.213 mol) in dry DMF (225 mL) was added triethylamine (60 mL, 0.425 mol) and stirred at RT for 15 min. The above reaction mixture was cooled to 0° C., added tritylchloride (59 g, 0.213 mol) followed by addition of catalytic amount of 4-DMAP (app. 20 mg) and allowed to stir at RT for 24 h. The reaction was diluted with water (100 mL), extracted with ethyl acetate (5×200 mL), dried and concentrated under vacuum. The crude was purified by column chromatography over silica gel (6% methanol in chloroform) to give the title compound (33 g, 34%). TLC: Chloroform/Methanol, 9:1, Rf=0.5

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795270B2
Source datasetuspto-grants-2010_09
ORD IDord-5c8e1ce56a3d40f986d532be54d21edd
Source noteuspto-grants-2010_09