HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428714Generated: October 26, 2026
Methyl 4-Formylbenzoate → Methyl 4-ethenylbenzoate
https://huagongshe.com/reaction/428714
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 4-Formylbenzoate | HCID 15294 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl 4-ethenylbenzoate | HCID 583124 | — |
Reaction Steps
To a stirred solution of n-butyllithium (4 mL, 2,5 M solution in hexane, 10 mmol) (Aldrich) in ether (30 mL) was added methyltriphenylphosphonium bromide (3.57 g, 10 mmol) (Aldrich) over a period of 5 min. The reaction mixture was stirred for 4 h at room temperature. To the resulting orange solution was added methyl 4-formylbenzoate (1.54 mL, 10 mmol) dropwise. The solution became colorless, and a white precipitate separated. The mixture was then heated to reflux and immediately allowed to cool to room temperature. The precipitate was removed by filtration. The resulting precipitate was washed with ether, and the combined ethereal filtrates were washed with water until neutral and then dried over anhydrous MgSO4. The solvent was removed and the residue, 4-ethenyl-benzoic acid methyl ester, was used in the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06313310B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-8693104f274b45b6a1977f38b376508b |
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| Source note | uspto-grants-2001_11 |
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