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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917374Generated: November 1, 2026

Dimethylformamide → HCID 69179367, compound

https://huagongshe.com/reaction/917374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant4-Methyl-2-phenylpyrimidine-5-carboxylic acidHCID 239975—
ReactantSodium BicarbonateHCID 516892—
Reactant4,4-Difluoro-3-Methyl-3-Buten-1-Yl MethanesulfonateHCID 23020237—
SolventWaterHCID 962—
ProductHCID 69179367HCID 6917936773.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

To 5 ml of N,N-dimethylformamide were dissolved 0.34 g (1.6 mmol) of 4-methyl-2-phenylpyrimidine-5-carboxylic acid, synthesized in accordance with a method described in “J. Chem. Soc.”, page 2183 (1923), and 0.30 g (1.5 mmol) of 4,4-difluoro-3-methyl-3-butenyl methanesulfonate, followed by the addition of 0.27 g (3.2 mmol) of sodium hydrogencarbonate and stirring at 100° C. for 3 hours. The reaction liquid was then poured in water and extracted with diethtyl ether. The organic layer was washed with water and a saturated saline solution in this order, followed by drying over anhydrous magnesium sulfate and concentration under reduced pressure. The residue was purified with silica gel column chromatography (diisopropyl ether:hexane=1:4) to obtain 0.35 g (yield: 73%) of 4,4-difluoro-3-methyl-3-butenyl 4-methyl-2-phenylpyrimidine-5-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273878B2
Source datasetuspto-grants-2007_09
ORD IDord-d5834e2f2f6d421982344909185c0bdf
Source noteuspto-grants-2007_09