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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957352Generated: October 31, 2026

Triethylamine → HCID 57325368, compound

https://huagongshe.com/reaction/1957352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPivalic anhydrideHCID 15234—
ReactantPivaloyl chlorideHCID 62493—
Reactant4-Phenoxyphenylacetic acidHCID 239077—
Reactant4-Methyl-5-phenyl-2-oxazolidinone, (4S,5R)-HCID 853161—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57325368HCID 5732536864.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution containing 4-phenoxyphenylacetic acid (10.0 g, 43.8 mmol) in THF (62.6 mL) at -78° C. was added pivaloyl chloride (5.49 g, 45.6 mmol) followed by triethylamine (4.61 g, 45.6 mmol). The mixture was stirred at -78° C. for 15 minutes, at 0° C. for 1 hour, then recooled to -78° C. In a separate flask, 2.5M n-butyllithium (20 mL, 50 mmol) was added to a solution of (4S,5R)-(-)-4-methyl-5-phenyl-2-oxazolidinone (8.86 g, 50 mmol) in THF (100 mL) at -78° C., stirred for 15 minutes, then transferred to the flask containing pivalic anhydride via cannula. The mixture was stirred 15 minutes at -78° C. then at room temperature for 18 hours. The solvent was removed, and the residue was partitioned between diethyl ether (500 mL) and 1N HCl (500 mL). The organic layer was dried (MgSO4), filtered and concentrated to provide a light yellow solid. The solid was chromatographed with 10% ethyl acetate in hexane to yield 10.9 g (64%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05783593
Source datasetuspto-grants-1998_07
ORD IDord-0bff963ec4474f05ab79cd840af3b348
Source noteuspto-grants-1998_07