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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12879Generated: October 26, 2026

Hydrochloric Acid → 5-chloro-1-cyclohexyl-1H-pyrazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/12879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTert-Butyl nitriteHCID 10906—
Reactantethyl 5-amino-1-cyclohexyl-1H-pyrazole-4-carboxylateHCID 351028—
CatalystCuprous chlorideHCID 62652—
SolventAcetonitrileHCID 6342—
Product5-chloro-1-cyclohexyl-1H-pyrazole-4-carboxylic acid ethyl esterHCID 6702092642%

Reaction Steps

Copper(I) chloride (2.500 g, 25.25 mmol) was suspended in 7.0 mL cold (ice/acetone bath) anhydrous acetonitrile. t-Butyl nitrite (5.75 mL, 90%, 43.56 mmol) was added, followed by a suspension of 5-amino-1-cyclohexyl-1H-pyrazole-4-carboxylic acid ethyl ester (4.408 g, 18.58 mmol) in 27.0 mL acetonitrile. The mixture was stirred at room temperature for 45 minutes and then at 70° C. for 1.25 hour. The mixture was cooled to room temperature, slowly added to 6N HCl (17.5 mL) and then extracted with methylene chloride. The organic phase was washed sequentially with water and brine. The aqueous phases were back extracted with a second portion of methylene chloride. The two organic phases were combined, dried over sodium sulfate and concentrated in vacuo. The crude residue was chromatographed by flash chromatography eluting with a gradient of 10-50% ethyl acetate/hexanes to give 5-chloro-1-cyclohexyl-1H-pyrazole-4-carboxylic acid ethyl ester (1.98 g; 42%). Mass spectrum: m/z: 257.3 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728029B2
Source datasetuspto-grants-2010_06
ORD IDord-b3919ed3436a4960839e99ad25df6759
Source noteuspto-grants-2010_06