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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189394Generated: October 30, 2026

Nitrogen → 2-(4-Bromo-pyrazol-1-ylmethyl)-oxazole-4-carboxylic acid

https://huagongshe.com/reaction/1189394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantSodium HydroxideHCID 14798—
Reactant2-(4-Bromo-pyrazol-1-ylmethyl)-oxazole-4-carboxylic acid ethyl esterHCID 67128429—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Bromo-pyrazol-1-ylmethyl)-oxazole-4-carboxylic acidHCID 67128466—

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 2-(4-bromo-pyrazol-1-ylmethyl)-oxazole-4-carboxylic acid ethyl ester (153 mg, 0.51 mmol) in THF (5.0 mL) was treated at rt with 1N NaOH (2.5 mL, 2.5 mmol) and the reaction mixture was stirred for 1 h at rt. The reaction mixture was poured in 1N HCl and extracted with EA. The org. extracts were dried over MgSO4, filtered, and the solvent was removed under reduced pressure to give the crude 2-(4-bromo-pyrazol-1-ylmethyl)-oxazole-4-carboxylic acid as a pale yellow solid. LC-MS-conditions 02: tR=0.72 min, [M+H]+=271.89.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674111B2
Source datasetuspto-grants-2014_03
ORD IDord-e719c9b094dc4490abf968d7e7eaba47
Source noteuspto-grants-2014_03