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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898830Generated: October 30, 2026

Aniline → HCID 11345649, compound

https://huagongshe.com/reaction/898830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantHCID 5365845HCID 5365845—
SolventTolueneHCID 1140—
ProductHCID 11345649HCID 1134564989%

Reaction Steps

A solution of 3-crotonoyl-1,3-oxazolidin-2-one (47 mg, 0.3 mmol) and Pd((R)-binap)(H2O)2(OTf)2 (8.0 mg, 0.0075 mmol) in toluene (1.5 ml) in a stream of nitrogen was cooled to 0° C., and aniline (42 mg, 0.45 mmol) was added. To the solution was dropwise added trifluoromethanesulfonic acid (63 μL, 0.45 mmol), and the resulting mixture was stirred at room temperature for 24 hours. When no starting material was detected, a saturated aqueous solution of ammonium chloride was added to quench the reaction, and the resulting mixture was extracted with ethyl acetate. The organic layer was concentrated and purified by a silica gel column chromatography (hexane:ethyl acetate=1:1) to give the objective 3-(3-phenylaminobutyryl)-oxazolidin-2-one (66 mg, 89% yield). The enantiomeric excess ratio was determined to be 94%. e.e. by a liquid chromatography with an optical isomer separating column (column: AD-H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351849B2
Source datasetuspto-grants-2008_04
ORD IDord-0fb49a1aa47042f48458837acf0ca3c9
Source noteuspto-grants-2008_04