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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360980Generated: October 31, 2026

2-(Methylamino)ethanol → HCID 86611439, compound

https://huagongshe.com/reaction/1360980

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Methylamino)ethanolHCID 8016—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Bromo-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-cyano-4-trifluoromethylsulfonylpyrazoleHCID 16727054—
SolventDimethylformamideHCID 6228—
ProductHCID 86611439HCID 8661143957.3%

Reaction Conditions

Temperature20 °C

Reaction Steps

Finely powdered potassium carbonate (7.29 g, 52.2 mmol) was added to a solution of 5-bromo-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-cyano-4-trifluoromethylsulphonylpyrazole (10.00 g, 19.3 mmol) in dry N,N-dimethylformamide (85 ml) and stirred for 1 hour at 20° C. 2-(Methylamino)ethanol (3.11 ml, 38.7 mmol) was then added and stirring continued for 2 hours at 20° C. The resulting mixture was poured into saturated ammonium chloride solution, extracted with ethyl acetate, and the organic layer washed with water and brine, dried (sodium sulfate), evaporated and purified by column chromatography eluting with hexane and ethyl acetate (2:1) to give 1-(2,6-dichloro-4-trifluoromethylphenyl)-3-cyano-5-[N-(2-hydroxyethyl)-N-methylamino]-4-trifluoromethylsulfonylpyrazole as a fine white powder (5.65 g, yield 57%), 19F-NMR: −63.7, −78.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879897B2
Source datasetuspto-grants-2011_02
ORD IDord-75b08a974a034458b20d6774f4fd8095
Source noteuspto-grants-2011_02