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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12870Generated: October 30, 2026

Ethanol → 1-tert-butyl-5-ethoxymethyl-1H-pyrazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/12870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium ethoxideHCID 2723922—
Reactant5-bromomethyl-1-tert-butyl-1H-pyrazole-4-carboxylic acid methyl esterHCID 67021009—
Product1-tert-butyl-5-ethoxymethyl-1H-pyrazole-4-carboxylic acid ethyl esterHCID 6702100551%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 5-bromomethyl-1-tert-butyl-1H-pyrazole-4-carboxylic acid methyl ester (220 mg, 0.79 mmol) in ethanol (4.0 mL, 0.2M) was treated with sodium ethoxide (65.4 mg, 0.96 mmol). The reaction mixture was warmed to 90° C. where it was stirred for 2.5 h. At this time, the reaction was concentrated in vacuo. The residue was partitioned between ethyl acetate (75 mL) and water (50 mL). The organics were washed with a saturated aqueous sodium bicarbonate solution (1×50 mL) and a saturated aqueous sodium chloride solution (1×50 mL), dried over magnesium sulfate, filtered and concentrated in vacuo to afford 1-tert-butyl-5-ethoxymethyl-1H-pyrazole-4-carboxylic acid ethyl ester (102.8 mg, 51%) as an orange oil. The material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728029B2
Source datasetuspto-grants-2010_06
ORD IDord-9b10de844b7a4ec5a9ee586191ff0421
Source noteuspto-grants-2010_06