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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713360Generated: October 25, 2026

3-Benzoyl-1-[(E)-4-(trityloxy)-2-butenyl]-1,2,3,4-tetrahydro-2,4-pyrimidinedione → 1-[(E)-4-trityloxy-2-butenyl]uracil

https://huagongshe.com/reaction/1713360

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Benzoyl-1-[(E)-4-(trityloxy)-2-butenyl]-1,2,3,4-tetrahydro-2,4-pyrimidinedioneHCID 59463758—
ReactantHCID 178418582HCID 178418582—
SolventMethanolHCID 887—
Product1-[(E)-4-trityloxy-2-butenyl]uracilHCID 1156804099.5%

Reaction Steps

Compound (12) (50 mg, 0.09 mmol) was dissolved and stirred at room temperature in a solution 0.2 M (5 ml) of MeONa in MeOH. The reaction was left at room temperature overnight, then the solution was neutralized with Dowex H+ ion exchange resin. The resin was filtered off and the filtrate was concentrated under reduced pressure to an oil which was purified by chromatography using CHCl3→CHCl3/MeOH 95:5 as gradient which gave the title compound as a white solid (38 mg, 90%). Rf: 0.51 in CHCl3/MeOH 90:10, M.p. 70-72° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795270B2
Source datasetuspto-grants-2010_09
ORD IDord-97b643140e8546eabf2e34ddd5143e4d
Source noteuspto-grants-2010_09