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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12884Generated: October 30, 2026

Water → 5-Chloro-1-(oxan-4-yl)-1h-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/12884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium HydroxideHCID 3939—
Reactant5-Chloro-1-(tetrahydro-pyran-4-yl)-1H-pyrazole-4-carboxylic acid ethyl esterHCID 67020853—
SolventMethanolHCID 887—
Product5-Chloro-1-(oxan-4-yl)-1h-pyrazole-4-carboxylic acidHCID 6702067799.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

5-Chloro-1-(tetrahydro-pyran-4-yl)-1H-pyrazole-4-carboxylic acid ethyl ester (2.194 g (98%), 8.31 mmol) was dissolved in methanol (12.5 mL). Lithium hydroxide (0.274 g, 11.44 mmol) and water (12.5 mL) were added and the mixture was heated at 80° C. for 1 hour. After cooling to room temperature, the mixture was concentrated to remove the methanol. Tetrahydrofuran was added to the residue and removed in vacuo to ensure complete removal of the methanol. The aqueous residue was treated with 6N HCl (1.88 mL) resulting in the precipitation of a thick milky solid. The solid was collected by filtration, washed with water and dried under high vacuum with heat to give 5-chloro-1-(tetrahydro-pyran-4-yl)-1H-pyrazole-4-carboxylic acid (1.900 g, 99%). Mass spectrum: m/z: 231.30 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728029B2
Source datasetuspto-grants-2010_06
ORD IDord-b4405faa9df24fa68cec7694e881028c
Source noteuspto-grants-2010_06