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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994096Generated: October 30, 2026

Trimethylsilyldiazomethane → methyl 5-chloro-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/1994096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant5-Chloro-1-Methyl-3-(Trifluoromethyl)-1H-Pyrazole-4-Carboxylic AcidHCID 2773806—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
Productmethyl 5-chloro-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylateHCID 1473689100%

Reaction Steps

To a solution of 5-chloro-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid (1.00 g, 4.38 mmol) in benzene (5.83 mL) and methanol (2.92 mL) at room temperature was added 2M trimethylsilyldiazomethane (8.75 mL). The resulting solution was stirred at room temperature for 3 hours. Solvent was removed at reduced pressure on a rotory evaporator to yield the title compound (1.06 g, 4.38 mmol, 100% yield) as a white solid. MS m/z 243 (MH+). 1H NMR (500 MHz, CHLOROFORM-D) δ ppm 3.82 (s, 3H) 3.89 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652004B2
Source datasetuspto-grants-2010_01
ORD IDord-de7e844bf95a4e8ba72c7580ae6d3089
Source noteuspto-grants-2010_01