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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043739Generated: October 29, 2026

Ethyl bromoacetate → ethyl 3,5-dichloro-1H-pyrazole-1-acetate

https://huagongshe.com/reaction/2043739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-dichloro-1H-pyrazoleHCID 20328069—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Productethyl 3,5-dichloro-1H-pyrazole-1-acetateHCID 6746397594.1%

Reaction Steps

A suspension of 3,5-dichloro-1H-pyrazole (690 mg, 5.0 mmol) (i.e. the product of Example 12, Step D), potassium carbonate (3 g, 21 mmol) in N,N-dimethylformamide (10 mL) was treated with ethyl bromoacetate (1.0 mL, 9.0 mmol) and stirred at ambient temperature for 12 h. The suspension was diluted with ethyl acetate, washed with water, and dried over MgSO4. The reaction mixture was then concentrated under reduced pressure giving 1.05 g of the title compound. This compound was of sufficient purity to use in subsequent reactions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586611B2
Source datasetuspto-grants-2013_11
ORD IDord-dd47032d9e9d4578891876cca7350dcc
Source noteuspto-grants-2013_11