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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353485Generated: October 26, 2026

Triethylamine → Methyl [(4-phenyl)-5-(3,4-dichlorophenyl)oxazole] 2-butanoate

https://huagongshe.com/reaction/353485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium AcetateHCID 517165—
ReactantMethyl 6-chloro-6-oxohexanoateHCID 520737—
Reactant2-(3,4-Dichlorophenyl)-2-hydroxy-1(phenyl)ethanoneHCID 22505260—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductMethyl [(4-phenyl)-5-(3,4-dichlorophenyl)oxazole] 2-butanoateHCID 13172342842,287.199%

Reaction Steps

5-(Methoxycarbonyl)pentanoyl chloride (2.82 g, 0.017 mol) and triethylamine (3.47 g, 0.034 mol) were added to a solution of 2-(3,4-dichlorophenyl)-2-hydroxy-1-[phenyl]ethanone (Step 1) (4.77 g, 0.017 mmol) in 40 mL of methylene chloride. The resulting mixture was stirred overnight at room temperature. The reaction mixture was diluted with 100 mL of methylene chloride. The organic solution was washed with water (1×100 mL), saturated brine (1×100 mL), dried over magnesium sulfate, filtered and concentrated. The concentrated residue was dried under high vacuum, then ammonium acetate (4.6 g, 0.06 mol) and 30 mL of acetic acid were added. The reaction mixture was heated at 100° C. for 2.5 h. The reaction mixture was cooled to room temperature, and the excess acetic acid was removed under vacuum. The resulting residue was partitioned between water (100 mL) and ethyl acetate (200 mL). The organic layer was separated, washed with saturated aqueous sodium bicarbonate (2×100 mL), saturated brine (1×100 mL), dried over magnesium sulfate, filtered and concentrated. The concentrated residue was purified by flash chromatography on silica gel (eluting with 1:9 ethyl acetate:hexane) to give 2.82 g (42.6%) of methyl [(4-phenyl)-5-(3,4-dichlorophenyl)oxazole]-2-butanoate as a yellow oil: HRMS calcd. for C20H17N1O3Cl2 390.0664. Found 390.0648.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06753344B2
Source datasetuspto-grants-2004_06
ORD IDord-578e0d5e455642b1bb1d0ce2a6b2ab7d
Source noteuspto-grants-2004_06