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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381253Generated: November 2, 2026

Triethylamine → HCID 58443666, compound

https://huagongshe.com/reaction/2381253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-(Difluoromethyl)-1-methyl-1 H-pyrazole-4-carbonyl chlorideHCID 15340110—
ReactantHCID 86657767HCID 86657767—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 58443666HCID 5844366654.3%

Reaction Steps

To a solution of O-ethyl-N-[1-methyl-2-(2,4,6-trichloro-phenyl)-ethyl]-hydroxylamine (0.5 g, 1.63 mmoles) in dichloromethane (5 ml) was added triethylamine (0.566 ml, 4.07 mmloes) followed by drop wise addition of a solution 3-difluoromethyl-1-methyl-1H-pyrazole-4-carbonyl chloride (0.34 g, 1.79 mmol) in dichloromethane at a temperature of 0° C. After the complete addition of acid chloride the mixture was stirred for 18 hours at ambient temperature. When the TLC confirmed completion of the reaction, the reaction mass was diluted with water and extracted with dichloromethane (3×60 ml). The combined dichloromethane layer were washed with 2N HCl, followed by saturated NaHCO3, then water and finally brine, dried over sodium sulfate and evaporated off solvent under reduced pressure. Resulting crude mass was purified by column chromatography using 60-120μ mesh silica gel and product collected at 30% ethyl acetate in hexane as eluent to give 3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxylic acid ethoxy-[1-methyl-2-(2,4,6-trichloro-phenyl)-ethyl]-amide (0.390 g, 50%) as off white solid. m.p: 111-114° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258169B2
Source datasetuspto-grants-2012_09
ORD IDord-9f99d6a157754c4cb3d1e017ac085b21
Source noteuspto-grants-2012_09