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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380430Generated: October 29, 2026

Water → 3-Methyl-5-(trifluoromethyl)dihydropyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/1380430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethylureaHCID 11719—
Reactant2-(Trifluoromethyl)prop-2-enoyl chlorideHCID 10149016—
SolventDimethylformamideHCID 6228—
Product3-Methyl-5-(trifluoromethyl)dihydropyrimidine-2,4(1H,3H)-dioneHCID 1300497930%
Product1-Methyl-5-(trifluoromethyl)dihydropyrimidine-2,4(1H,3H)-dioneHCID 1300498010%

Reaction Steps

A solution of methylurea (148 mg; 2.0 mmoles) in DMF (2 ml) was cooled to 0° C., and α-trifluoromethylacryloyl chloride (317 mg; 2.0 mmoles) was added dropwise. The mixture was stirred at room temperature for 1 hour, and water (20 ml) was added. The mixture was extracted with methylene chloride (20 ml×1, 10 ml×2). The combined extracts were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by a column chromatography on silica gel (chloroform:ethyl acetate=3:1) to give 39 mg (yield: 10%) of 1-methyl-5-trifluoromethyl-5,6-dihydrouracil (OF-3) and 117 mg (yield: 30%) of 3-methyl-5-trifluoromethyl-5,6-dihydrouracil (OF-2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04581452
Source datasetuspto-grants-1986_04
ORD IDord-cbc7d333692443de91618c2cf3611781
Source noteuspto-grants-1986_04