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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294109Generated: November 3, 2026

Triethylamine → HCID 54429599, compound

https://huagongshe.com/reaction/2294109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Fluorobenzoic acidHCID 9935—
ReactantOxalyl chlorideHCID 65578—
Reactant2-Bromoethylamine hydrobromideHCID 2774217—
CatalystDimethylformamideHCID 6228—
SolventBenzeneHCID 241—
SolventDichloromethaneHCID 6344—
ProductHCID 54429599HCID 5442959942.5%

Reaction Steps

A mixture of 2-fluorobenzoic acid (4.5 g, 32.14 mmol) and oxalyl chloride (4.1 mL, 48.2 mL) in 2 drops of DMF and 40 mL of methylene chloride was heated at reflux for 2 hours. The mixture was allowed to cool to room temperature and stirred for approximately 12 hours and then the solvents were removed by rotary evaporation. The residue was slowly added to a suspension of 2-bromoethylamine hydrobromide (5.7 g, 28 mmol) and triethylamine (21 mL, 160 mmol) in 200 mL of benzene. The mixture was heated at reflux for 12 hours, allowed to cool to room temperature and then stirred for an additional 12 hours. The mixture was quenched with water and the aqueous layer was separated and extracted with methylene chloride (2×50 mL). The combined extracts were dried (MgSO4) and concentrated. The residue was purified on silica gel by column chromatography eluting with hexanes/ethyl acetate (5:1) to give 2-fluoro-1-(4,5-dihydrooxazol-2-yl)benzene (1.96 g, 11.9 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688795
Source datasetuspto-grants-1997_11
ORD IDord-1f719d512db74bdc89712918749eda29
Source noteuspto-grants-1997_11