Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452104Generated: October 27, 2026

Sodium Hydroxide → 5-ethyl-1-methyl-1H-pyrazole-3-carboxylic acid

https://huagongshe.com/reaction/1452104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 5-ethyl-1-methyl-1H-pyrazole-3-carboxylateHCID 22145397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product5-ethyl-1-methyl-1H-pyrazole-3-carboxylic acidHCID 1996759447%

Reaction Steps

Ethyl 5-ethyl-1-methylpyrazole-3-carboxylate (6.86 g) in ethanol (70 ml) was treated with sodium hydroxide (1.58g) in water (30 ml) and heated under reflux for 6 h. The solution was concentrated and the aqueous phase washed with ethyl acetate before adding dichloromethane (50 ml). The solution was acidified with 5M hydrochloric acid, and the mixture exhaustively extracted with dichloromethane. The remaining undissolved solid was filtered off suspended in water and the pH adjusted to 6 with saturated sodium hydrogen carbonate. The solution was again extracted with dichloromethane. The combined organic layers were dried over anhydrous magnesium sulphate and concentrated to give the title compound as a white solid, (2.72g, 47%); (Found: M+, 154.0742. C7H10N2O2 requires M, 154.0742); nmax (CH2Cl2) 3689 and 1760 cm-1 ; dH (CDCl3) 1.30 (3H, t, J7.4 Hz), 2.64 (2H, q, J7.4 Hz), 3.88 (3H, s) and 6.65 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05606051
Source datasetuspto-grants-1997_02
ORD IDord-7cc63069e0ce4353ad26c2b45e90da4f
Source noteuspto-grants-1997_02