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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225418Generated: October 30, 2026

Hydrochloric Acid → N-allyloxy-3,5-dichloro-1-methylpyrazole-4-carboxylic acid amide

https://huagongshe.com/reaction/225418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-Dichloro-1-methylpyrazole-4-carbohydroxamic acidHCID 57752427—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductN-allyloxy-3,5-dichloro-1-methylpyrazole-4-carboxylic acid amideHCID 5775242872.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

In a solution of potassium carbonate (15.8 g, 114 mmol) in water (60 ml), a solution of 3,5-dichloro-1-methylpyrazole-4-carbohydroxamic acid (20.0 g, 95.2 mmol) and allyl bromide (13.8 g, 114 mmol) in toluene (60 ml) was added, and stirred at 50° C. for 3 hours. After cooling to room temperature, the mixture was adjusted to pH 1 by adding 35% hydrochloric acid, precipitated solid was filtered off, washed with water and toluene in that order, and dried to obtain the aimed product (17.2 g). Melting point 96-97° C. Proton nuclear magnetic resonance chemical shift values δ (ppm) (in CDCl3) 3.84 (s, 3H), 4.51 (d, J=6.3 Hz, 2H), 5.3-5.46 (m, 2H), 5.94-6.13 (m, 1H), 8.80 (brs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557067B2
Source datasetuspto-grants-2009_07
ORD IDord-88d79534543f45ca8f26511391ec5734
Source noteuspto-grants-2009_07