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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523885Generated: October 31, 2026

1,1'-Carbonyldiimidazole → (S)-(+)-5,5-Dimethyl-4-phenyl-2-oxazolidinone

https://huagongshe.com/reaction/523885

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant(S)-1-amino-2-methyl-1-phenylpropan-2-olHCID 46941324—
SolventDichloromethaneHCID 6344—
Product(S)-(+)-5,5-Dimethyl-4-phenyl-2-oxazolidinoneHCID 2733820—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of C2 (38.8 g, 235 mmol) in dichloromethane (1000 mL) was treated with carbonyldiimidazole (45.6 g, 281 mmol) and heated at reflux for 2 hours. The reaction mixture was cooled to 25° C., quenched with 1 N hydrochloric acid (560 mL), and extracted with dichloromethane (3×). The combined organic extracts were dried over sodium sulfate and concentrated, and the resultant residue was purified by trituration with 4:1 hexanes:ethyl acetate, followed by chromatography on silica gel (gradient: 9:1 hexanes:ethyl acetate to 1:1 hexanes:ethyl acetate) to provide C3 as a white solid. Yield: 24.7 g, 55%. MS (APCI) m/z 192.2 (M+1). 1H NMR (400 MHz, CDCl3) δ 0.91 (3H, s), 1.58 (3H, s), 4.62 (1H, s), 5.53-5.60 (1H, br s), 7.20-7.39 (5H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340493B2
Source datasetuspto-grants-2016_05
ORD IDord-31f0f5c110c046e2a6cd54d4c8bb2dd9
Source noteuspto-grants-2016_05