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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206459Generated: October 31, 2026

Hydrochloric Acid → 1-benzyl-5-methyl-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/2206459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactantmethyl 1-benzyl-5-methyl-1H-pyrazole-4-carboxylateHCID 89741686—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product1-benzyl-5-methyl-1H-pyrazole-4-carboxylic acidHCID 649317640.3%

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of methyl 1-benzyl-5-methyl-1H-pyrazole-4-carboxylate (200 mg, 0.86 mmol), lithium hydroxide monohydrate (111 mg, 2.62 mmol), tetrahydrofuran (10 mL), methanol (2 mL) and water (2 mL) was stirred at 20° C. for 4 hours. The mixture was acidified to pH=1 with concentrated hydrochloric acid and then extracted with ethyl acetate (15 mL×3). The combined organic phase was dried by sodium sulfate, and then filtered. The filtrate was concentrated in vacuo and separated by chiral HPLC (condition: column AD-H (20 mm*250 mm*5 μm), hexane: ethanol (0.2% DEA)=50:50, flow rate: 13 mL/min) to give 1-benzyl-5-methyl-1H-pyrazole-4-carboxylic acid (75 mg, 40%). LRMS (M+H+) m/z: calcd. 216.09. found 216.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371331B2
Source datasetuspto-grants-2016_06
ORD IDord-5303fb3f1a134a3f9b640c92bf9cef1b
Source noteuspto-grants-2016_06