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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116616Generated: November 1, 2026

Ethyl Acetate → HCID 11428608, compound

https://huagongshe.com/reaction/2116616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantValeryl chlorideHCID 61186—
ReactantHCID 69185427HCID 69185427—
SolventDichloromethaneHCID 6344—
ProductHCID 11428608HCID 1142860834%

Reaction Conditions

Temperature40 °C

Reaction Steps

12.6 g of 2-[(4-bromobenzylidene)amino]-3-methylbutyric acid sodium salt (41.1 mmoles) are suspended in 80 ml of dry dichloromethane. The mixture is refluxed (40° C.), under slight nitrogen stream. 7.9 g of valeryl chloride (65.5 mmoles) are added. After 2 hours under reflux, the mixture is cooled to 25° C. The organic phase is washed three times with 50 ml of water and concentrated under reduced pressure, at 25-30° C., to obtain an oily residue. 50 ml of ethyl acetate are added and the organic phase is washed with a weakly basic NaOH solution and/or with water to neutrality. The organic phase is washed with a sodium bisulfite solution. The organic phase is washed with water and dried over sodium sulfate, filtered and evaporated under reduced pressure. The oily residue is taken up with ethanol from which the product crystallizes as a white solid. 2-(4-Bromophenyl)-4-isopropyl-3-pentanoyl-oxazolidin-5-one is obtained (5.2 g; 14.1 mmoles; molar yield: 34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439261B2
Source datasetuspto-grants-2008_10
ORD IDord-2ccadb3ab97a4797bdbce53d333f0535
Source noteuspto-grants-2008_10