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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020343Generated: November 2, 2026

Hydrochloric Acid → 2-Bromo-4-(trifluoromethyl)-1,3-oxazole-5-carboxylic acid

https://huagongshe.com/reaction/1020343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantEthyl 2-bromo-4-(trifluoromethyl)-1,3-oxazole-5-carboxylateHCID 53403202—
SolventOxolane--water (1/1)HCID 21881883—
SolventWater ethylacetateHCID 22728543—
Product2-Bromo-4-(trifluoromethyl)-1,3-oxazole-5-carboxylic acidHCID 5746178988.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

LiOH.H2O (0.64 g, 15.25 mmol) was added to a solution of ethyl 2-bromo-4-trifluoromethyloxazole-5-carboxylate (A-2) (3.50 g, 12.2 mmol) in THF/H2O (20/5 mL) at 0° C. followed by stirring for 3 h at 0° C. The reaction mixture was diluted with EtOAc/H2O (25/25 mL) and neutralized with 1 M HCl (16 mL) at 0° C. The organic phase was separated, dried over MgSO4, filtered, and concentrated. The product was dried in vacuo to yield 2-bromo-4-trifluoromethyloxazole-5-carboxylic acid (A-38) as a white solid (2.80 g, 88% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716312B2
Source datasetuspto-grants-2014_05
ORD IDord-19fd433f5dfc4a29a3f71291672a81eb
Source noteuspto-grants-2014_05