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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467969Generated: October 30, 2026

Triethylamine → HCID 131731126, compound

https://huagongshe.com/reaction/467969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-(Difluoromethyl)-1-methyl-1 H-pyrazole-4-carbonyl chlorideHCID 15340110—
ReactantHCID 44595679HCID 44595679—
SolventDichloromethaneHCID 6344—
ProductHCID 131731126HCID 131731126—

Reaction Steps

At a temperature of 0° C., a solution of 3-difluoromethyl-1-methyl-1H-pyrazole-4-carbonyl chloride (0.243 g; 1.24 mmol) in dichloromethane (5 ml) was added dropwise to a stirred solution of (S)-2-(2,4,6-trichloro-phenoxymethyl)-pyrrolidine hydrochloride (0.35 g; 1.24 mmol), which was prepared as described in example P12, and triethylamine (0.35 ml; 2.48 mmol) in dichloromethane (10 ml). The ice bath was removed and reaction mixture was allowed stirring for 3 hours. The reaction mixture was washed with 1M NaOH (10 ml), 2M HCl (10 ml) and saturated NaCl (50 ml) and then dried over Na2SO4. After removal of the solvent, the residue (0.45 g in the form of an oil) was purified by flash chromatography over silica gel (eluent:cyclohexane/ethyl acetate 2:8). 0.27 g (50% of theory) of 3-difluoromethyl-1-methyl-1H-pyrazol-4-yl)-[(S)-2-(2,4,6-trichloro-phenoxymethyl)-pyrrolidin-1-yl]-methanone was obtained in form of an oil which solified after standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623902B2
Source datasetuspto-grants-2014_01
ORD IDord-d3026b70012d4cb1b0fd8497d4ff2b66
Source noteuspto-grants-2014_01