Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1153843Generated: October 26, 2026

Water → Ethyl 2,4-dimethyl[1,1'-biphenyl]-3-carboxylate

https://huagongshe.com/reaction/1153843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhenylacetaldehydeHCID 998—
ReactantMorpholineHCID 8083—
Reactantethyl 4,6-dimethyl-2-oxo-2H-pyran-5-carboxylateHCID 76918—
SolventTolueneHCID 1140—
ProductEthyl 2,4-dimethyl[1,1'-biphenyl]-3-carboxylateHCID 1312628955.6%

Reaction Steps

A stirred solution of phenylacetaldehyde (77.0 g, 0.64 mole) and morpholine (56.0 g, 0.64 mole) in toluene (500 ml) was heated at reflux until the theoretical amount of water was collected in a Dean-Stark trap. The reaction mixture was cooled slightly, and ethyl 4,6-dimethyl-2-oxo-2H-pyran-5-carboxylate (125.0 g, 0.64 mole) was added. The solvent was distilled from the reaction mixture at atmospheric pressure to leave a residue. The residue was then heated at 200° for 2.5 hours. A Dean-Stark trap was used to collect the distilled morpholine. The remaining pot residue was cooled and slurried with a mixture of silica gel (700 g) and methylene chloride (1500 ml) for 45 minutes. The slurry was filtered and the filter cake rinsed with methylene chloride (500 ml). The combined filtrates were evaporated under reduced pressure to leave a thick brown residue. This residue was distilled under reduced pressure to give several fractions. All fractions which contained more than 73% product by gc analysis were combined to give a total of 90.5 g crude ethyl 2,4-dimethyl-[1,1'-biphenyl]-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04486588
Source datasetuspto-grants-1984_12
ORD IDord-34562dd3138241a699e716d8cd4ad8fd
Source noteuspto-grants-1984_12