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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525348Generated: October 30, 2026

Ethyl Acetate → HCID 89814050, compound

https://huagongshe.com/reaction/525348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 89827451HCID 89827451—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 89814050HCID 89814050—

Reaction Steps

To a solution of (S)-tert-butyl (2-hydroxy-2-methyl-1-(o-tolyl)propyl)carbamate (1 g, 3.5 mmol) in THF (20 mL) was added potassium tert-butoxide (803.37 mg, 7.1 mmol) at 0-5° C. The resulting reaction mixture was stirred for 2 hours at ambient temperature. After completion of the reaction (monitored by TLC, TLC system: 50% EtOAc in hexane), the reaction mixture was quenched with ice water and extracted with EtOAc. The combined organic layers were washed with, water, washed with saturated NaCl solution, dried with Na2SO4, filtered and evaporated to afford (S)-5,5-dimethyl-4-(o-tolyl)oxazolidin-2-one, 0.7 g (95.28% Y) as an off-white solid. 1H NMR (400 MHz, DMSO-d6): δ 7.96 (s, 1H), 7.27-7.25 (m, 1H), 7.22-7.19 (m, 3H), 4.83 (s, 1H), 2.29 (s, 3H), 1.55 (s, 3H), 0.81 (s, 3H). m/z (ESI) 206.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340549B2
Source datasetuspto-grants-2016_05
ORD IDord-eb3a8d11acdf48139ae7c40f6f8fbc01
Source noteuspto-grants-2016_05