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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898827Generated: October 31, 2026

Aniline → HCID 11345649, compound

https://huagongshe.com/reaction/898827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantMethanesulfonic AcidHCID 6395—
ReactantHCID 5365845HCID 5365845—
SolventEthyl AcetateHCID 8857—
ProductHCID 11345649HCID 1134564915%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-crotonoyl-1,3-oxazolidin-2-one (155 mg, 1.0 mmol) in ethyl acetate (3 ml) in a stream of nitrogen was added Pd((R)-binap)(H2O)2(OTf)2 (26.6 mg, 0.025 mmol), and the resulting mixture was cooled to 0° C. Aniline (0.11 ml, 1.2 mmol) was added to the mixture, and to the solution was added slowly methanesulfonic acid (0.078 ml, 1.2 mmol). Then, the cooling ice-bath was removed and the reaction mixture was reacted at room temperature for 18 hours with stirring. After completion of the reaction, the solvent was evaporated off, and the crude product obtained was purified by a silica gel column chromatography (hexane:ethyl acetate=1:1) to give the objective compound 3-(3-phenylaminobutyryl)-oxazolidin-2-one (37 mg, 15% yield). Enantiomeric excess ratio of this product was determined by a liquid chromatography using a column for separation of optical isomers (column: AD-H) to be 82% e.e.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351849B2
Source datasetuspto-grants-2008_04
ORD IDord-4e21057441bd464b81c919238e62c8f9
Source noteuspto-grants-2008_04