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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380426Generated: November 1, 2026

N,N'-Dimethylurea → 1,3-Dimethyl-5-(trifluoromethyl)dihydropyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/1380426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DimethylureaHCID 7293—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-(Trifluoromethyl)acrylic acidHCID 587694—
SolventDimethylformamideHCID 6228—
Product1,3-Dimethyl-5-(trifluoromethyl)dihydropyrimidine-2,4(1H,3H)-dioneHCID 1300497857%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of α-trifluoromethylacrylic acid (700 mg; 5.0 mmoles) and 1,3-dimethylurea (419 mg; 4.8 mmoles) in DMF (5 ml) was cooled to 0° C., and then a solution of DCC (1.21 g; 5.9 mmoles) in DMF (3 ml) was added dropwise. The mixture was stirred at 0° C. for 1 hour. The precipitated solid was filtered off, and washed with ethyl acetate. The solvents were evaporated under reduced pressure from the combined filtrates. The residue was purified by a column chromatography on silica gel to give 566 mg (yield 57%) of 1,3-dimethyl-5-trifluoromethyl-5,6-dihydrouracil (OF-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04581452
Source datasetuspto-grants-1986_04
ORD IDord-142e95b292f3494399368b17141eba84
Source noteuspto-grants-1986_04