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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 570183Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/570183

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuryl chlorideHCID 24648—
Eduktethyl 3-(tert-butyl)-1-methyl-1H-pyrazole-5-carboxylateHCID 2799344—
LösungsmittelDichloromethaneHCID 6344—
Produktethyl 3-tert-butyl-4-chloro-1-methyl-1H-pyrazole-5-carboxylateHCID 67412028—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09023846B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-5f61c25fc0fd4378b046af5a34fad283
Quellennotizuspto-grants-2015_05