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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630661Generated: November 2, 2026

tert-Butyl methyl ether → ethyl 3-(bromoacetyl)-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylate

https://huagongshe.com/reaction/1630661

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl methyl etherHCID 15413—
ReactantBromineHCID 24408—
Reactant1,4-DioxaneHCID 31275—
Reactantethyl 3-acetyl-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylateHCID 66587473—
SolventWaterHCID 962—
Productethyl 3-(bromoacetyl)-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylateHCID 86661386—

Reaction Steps

1.20 g (4.40 mmol) of ethyl 3-acetyl-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylate were initially charged in in each case 30 ml of dioxane and methyl tert-butyl ether and 776 mg (4.85 mmol) of bromine were added dropwise at RT. The mixture was then stirred under reflux for 6 h. The reaction mixture was added to water, and the organic phase was separated off, dried over sodium sulphate and concentrated. The residue was recrystallized from methyl tert-butyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791139B2
Source datasetuspto-grants-2014_07
ORD IDord-9378d0a888894f969763d0eaa51dcc3b
Source noteuspto-grants-2014_07