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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1153842Generated: October 25, 2026

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

https://huagongshe.com/reaction/1153842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactantethyl 4,6-dimethyl-2-oxo-2H-pyran-5-carboxylateHCID 76918—
Reactant4-(2-Phenylethenyl)morpholineHCID 54492098—
SolventTolueneHCID 1140—
ProductEthyl 2,4-dimethyl[1,1'-biphenyl]-3-carboxylateHCID 1312628918.1%

Reaction Steps

Under a dry nitrogen atmosphere a solution of commercial ethyl 4,6-dimethyl-2-oxo-2H-pyran-5-carboxylate (19.6 g, 0.1 mole) in toluene (20 ml) was added dropwise to a stirred solution of 4-(2-phenylethenyl)morpholine (14.3 g, 0.076 mole) in toluene (200 ml). Preparation of the morpholine derivative is described in U.S. Pat. No. 3,922,237. After the addition, the reaction mixture was heated at reflux for approximately 20 hours. The reaction mixture was then cooled and concentrated under reduced pressure, leaving a residue. The residue was heated at 170° under a dry nitrogen atmosphere for 3.5 hours, allowed to cool to room temperature, and then filtered. The filtrate was purified by column chromatography on silica gel, elution first with n-hexane: ethyl acetate, and finally ethyl acetate, to give ethyl 2,4-dimethyl-[1,1'-biphenyl]-3-carboxylate (3.5 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04486588
Source datasetuspto-grants-1984_12
ORD IDord-e52eceddde834449b16106a075d0035c
Source noteuspto-grants-1984_12