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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481503Generated: November 2, 2026

Sulfuryl chloride → ethyl 3-tert-butyl-4-chloro-1-methyl-1H-pyrazole-5-carboxylate

https://huagongshe.com/reaction/1481503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
Reactantethyl 3-(tert-butyl)-1-methyl-1H-pyrazole-5-carboxylateHCID 2799344—
SolventDichloromethaneHCID 6344—
Productethyl 3-tert-butyl-4-chloro-1-methyl-1H-pyrazole-5-carboxylateHCID 67412028—

Reaction Steps

To a solution of 5-tert-butyl-2-methyl-pyrazole-3-carboxylic acid ethyl ester (2.10 g, 10.0 mmol) in 25 mL of DCM was added sulfuryl chloride (1.05 mL, 13.0 mmol) slowly under Ar. After stirring at room temperature for 3 h under Ar, the resulting mixture was treated with DCM (30 mL), washed with ice H2O, saturated aqueous NaHCO3 and brine, and dried with Na2SO4. Removal of the solvent under reduced pressure yielded the title compound as a white solid. 1H-NMR (400 MHz, CDCl3) δ: 4.40 (q, J=7.2 Hz, 2H), 4.07 (s, 3H), 1.42 (t, J=7.2 Hz, 3H), 1.40 (s, 9H). Mass Spectrum (LCMS, ESI pos.) Calculated For C11H17ClN2O2: 245.1 (M+H). Measured: 245.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409915B2
Source datasetuspto-grants-2016_08
ORD IDord-e18ad5db4a8647c5afdccdfb2abd5d1a
Source noteuspto-grants-2016_08