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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164731Generated: November 2, 2026

2-(4-chloro-2-fluoro-5-(2-propynyloxy)phenyl]-4-methyl-1,2,4-triazine-3.5(2H,4H)-dione → HCID 19863061, compound

https://huagongshe.com/reaction/1164731

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-chloro-2-fluoro-5-(2-propynyloxy)phenyl]-4-methyl-1,2,4-triazine-3.5(2H,4H)-dioneHCID 14276952—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 19863061HCID 1986306174%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 1.6 g (0.0052 mole) of 2-(4-chloro-2-fluoro-5-(2-propynyloxy)phenyl]-4-methyl-1,2,4-triazine-3.5(2H,4H)-dione (compound 21) dissolved in 5 mL of glacial acetic acid was added dropwise to a stirred suspension of 1.5 g (0.023 mole) of zinc dust in 10 mL of glacial acetic acid and 5 mL of water. After complete addition the mixture was heated at 60° C. for 1.5 hours. The mixture was filtered and the filtrate was partitioned between 50 mL of water and 50 mL of diethyl ether. The organic phase was washed first with water followed by a saturated aqueous sodium bicarbonate solution. The washed organic phase was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure to yield 1.2 g of 2-[4-chloro-2-fluoro-5-(2-propynyloxy)phenyl]-1,6-dihydro-4-methyl-1,2,4-triazine-3,5(2H,4H)-dione as an oil, compound A-3 of Table A-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04906287
Source datasetuspto-grants-1990_03
ORD IDord-197c743dfdce4b2bbd4438a1ac0cbc3f
Source noteuspto-grants-1990_03