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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807392Generated: November 1, 2026

Triethylamine → HCID 131730171, compound

https://huagongshe.com/reaction/1807392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbonyl chlorideHCID 2794581—
ReactantHCID 86669075HCID 86669075—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 131730171HCID 13173017185.9%

Reaction Steps

To a stirred solution of trans O-methyl-N-{1-[2-(2,4,5-trichloro-thiophen-3-yl)-cyclopropyl]ethyl}-hydroxylamine (0.25 g; 0.83 mmol) prepared as described in example P17 and triethylamine (0.16 ml; 1.08 mmol) in dichloromethane (5.0 ml) at ambient temperature was added dropwise 1-methyl-3-trifluoromethyl-1H-pyrazole-4-carbonyl chloride (0.18 g; 0.83 mmol). The reaction mixture was stirred for 16 hours at ambient temperature then poured in water (3 ml) and extracted with dichloromethane (3×1 ml). Combined organic layers were washed with water (1 ml), brine and dried over anhydrous sodium sulphate. The solvent was removed in vacuo and the residue was purified by flash chromatography over silica gel (elution gradient: cyclohexane/ethyl acetate 99:1 to 30:70) to afford 0.34 g (85% of theory) of trans 1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid methoxy-{1-[2-(2,4,5-trichloro-thiophen-3-yl)-cyclopropyl]-ethyl}-amide as a resin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357635B2
Source datasetuspto-grants-2013_01
ORD IDord-2edb4dd76a814a4195a2e0e784580229
Source noteuspto-grants-2013_01