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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225409Generated: October 30, 2026

Potassium Carbonate → Methyl 2-[2-[4-(4-methyl-1,2,4-triazine-3,5-dion-2-yl)-3-fluorophenoxymethyl]-5-methylphenoxy]propionate

https://huagongshe.com/reaction/2225409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-(2-chloromethyl-5-methylphenoxy)propionateHCID 15765398—
Reactant2-(4-Hydroxy-2-fluorophenyl)-4-methyl-1,2,4-triazine-3,5-dioneHCID 18981067—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-[2-[4-(4-methyl-1,2,4-triazine-3,5-dion-2-yl)-3-fluorophenoxymethyl]-5-methylphenoxy]propionateHCID 350294578.9%

Reaction Steps

By the method of Example 1, Step I, 0.47 g (0.002 mole) of 2-(4-hydroxy-2-fluorophenyl)-4-methyl-1,2,4-triazine-3,5-dione and 0.73 g (0.003 mole) of methyl 2-(2-chloromethyl-5-methylphenoxy)propionate were reacted in the presence of 0.41 g (0.003 mole) of anhydrous potassium carbonate in 30 mL of N,N-dimethylformamide, yielding 0.70 g of methyl 2-[2-[4-(4-methyl-1,2,4-triazine-3,5-dion-2-yl)-3-fluorophenoxymethyl]-5-methylphenoxy]propionate as a syrup. The IR and NMR spectra were consistent with the proposed structure. NMR: 1.60 (d, 3H, JHH =8.0 Hz); 2.30 (s, 3H); 3.40 (s, 3H); 3.78 (s, 3H); 4.84 (q, 1H, JHH =8.0 Hz); 5.18 (dd, 2H, JHH =10 Hz); 6.58 (s, 1H); 6.8-7.3 (m, 5H); 7.54 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344812
Source datasetuspto-grants-1994_09
ORD IDord-cb126c6dabb3443e8446b28f19bda49c
Source noteuspto-grants-1994_09