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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908512Generated: October 26, 2026

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

https://huagongshe.com/reaction/908512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-BenzoyluracilHCID 569513—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant(E)-4-(Trityloxy)but-2-en-1-olHCID 10882092—
SolventTetrahydrofuranHCID 8028—
SolventEthyl acetate hexaneHCID 21226206—
Product3-Benzoyl-1-[(E)-4-(trityloxy)-2-butenyl]-1,2,3,4-tetrahydro-2,4-pyrimidinedioneHCID 5946375848%

Reaction Steps

Polymer bound triphenylphosphine (0.75 g, 2.25 mmol) was shaken in THF (5 ml) for 15 minutes, then 3-benzoyluracil (290 mg, 1.35 mmol), trityl alcohol (11) (300 mg, 0.90 mmol) were added to the suspension of the resin. A solution of DIAD (0.354 ml, 1.80 mmol) in THF (2 ml) was added to the mixture. The reaction was shaken 24 hours at room temperature and monitored by TLC (Hexane/EtOAc 50:50). The resin was filtered and washed twice with THF (5 ml). The filtrate was concentrated under reduced pressure and taken in EtOAc (5 ml), a white solid precipitated. The precipitate was filtered; the filtrate was concentrated again and purified by flash chromatography using Hexane/EtOAc 40:60→60:40 as gradient which gave the title compound as a white foam (222 mg, 48%). Rf: 0.55 in Hexane/EtOAc 50:50 (UV/PMA).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017620B2
Source datasetuspto-grants-2011_09
ORD IDord-fe0d7a7efd334c18a899370df3e07154
Source noteuspto-grants-2011_09