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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400533Generated: October 29, 2026

Hydrochloric Acid → HCID 59504626, compound

https://huagongshe.com/reaction/2400533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
Reactantp-Xylyl bromideHCID 7721—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 68509351HCID 68509351—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 59504626HCID 5950462618%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a mechanically stirred solution of methyl 5-ethyl-4-methyl-1H-pyrazole-3-carboxylate hydrochloride (Step 1, 825 mg, 4.03 mmol) in dry ethanol (20 mL) was added potassium tert-butoxide (1.18 g, 10.5 mmol) and a solution of 4-methylbenzyl bromide (1.12 g, 6.05 mmol) in dry ethanol (20 mL). The reaction mixture was stirred at 60° C. over night. After being cooled to rt, LiOH (0.5N aq., 40.3 mL, 20.1 mmol) was added, and the mixture was stirred at 40° C. for additional 3 h. After being cooled to RT again, the reaction mixture was diluted with water (200 mL) and acidified with HCl (2N aq., 12.1 mL, 24.2 mmol). Extraction with dichloromethane, drying over anhydrous magnesium sulfate, filtration, evaporation of the solvent and subsequent purification by preparative HPLC afforded the title compound as a white solid (183 mg, 18%): 1H NMR (400 MHz, CDCl3) δ 7.12 (d, 2H), 7.01 (d, 2H), 5.30 (s, 2H), 2.53 (quart, 2H), 2.32 (s, 3H), 2.22 (s, 3H), 0.98 (t, 3H); ES-MS m/z 259 (MH)+; HPLC RT (Method D) 2.13 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796253B2
Source datasetuspto-grants-2014_08
ORD IDord-86580bfd48154359b5ffbb889d691588
Source noteuspto-grants-2014_08