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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078465Generated: October 30, 2026

Ethyl Bromide → HCID 22618612, compound

https://huagongshe.com/reaction/1078465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantMagnesiumHCID 5462224—
ReactantHCID 22618561HCID 22618561—
ReactantHCID 178418443HCID 178418443—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 22618612HCID 22618612—

Reaction Steps

A solution of ethyl magnesium bromide, prepared from magnesium (0.57 g) and ethyl bromide (2.6 g) in dry diethyl ether (25 ml), was added dropwise to a stirred solution of 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-thiocyanato-3-trifluoromethylpyrazole (5.0 g) in dry ether (50 ml) at -20° C. After stirring for a further 2 hours at room temperature, water (130 ml) was carefully added, and stirring maintained for 0.25 hour. The ether layer was separated, dried over anhydrous magnesium sulphate, and evaporated in vacuo to give a yellow gum. Purification by chromatography on silica (Merck 230-400 mesh, 0.7 kg cm-2) eluting with dichloromethane-petroleum ether (1:1) gave a product, which recrystallized from hexane to furnish 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-ethylthio-3-trifluoromethylpyrazole, in the form of white needles, m.p. 116°-116.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05547974
Source datasetuspto-grants-1996_08
ORD IDord-4031cfd191ed4c5e9d6f824f3ff23dc7
Source noteuspto-grants-1996_08