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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | ethyl 4,6-dimethyl-2-oxo-2H-pyran-5-carboxylate | HCID 76918 | — |
| Reactant | 4-(2-Phenylethenyl)morpholine | HCID 54492098 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 2,4-dimethyl[1,1'-biphenyl]-3-carboxylate | HCID 13126289 | 18.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04486588 |
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| Source dataset | uspto-grants-1984_12 |
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| ORD ID | ord-e52eceddde834449b16106a075d0035c |
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| Source note | uspto-grants-1984_12 |
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