HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412255Generated: October 31, 2026
Isopropenyl acetate → Methyl [3-(2-oxopropyl)phenyl]acetate
https://huagongshe.com/reaction/2412255
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropenyl acetate | HCID 7916 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Methyl 2-(3-bromophenyl)acetate | HCID 11746402 | — |
| Reactant | Methoxytri-n-butylstannane | HCID 11964040 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl [3-(2-oxopropyl)phenyl]acetate | HCID 21035403 | 66.5% |
Reaction Steps
A stirred mixture of methyl (3-bromophenyl)acetate (19.7 g, 86.0 mmol), tributyltin methoxide (37.1 mL, 129 mmol), isopropenyl acetate (14.2 mL, 129 mmol), palladium acetate (961 mg, 4.28 mmol), and tri-o-tolylphosphine (2.63 g, 8.64 mmol) in toluene (70 mL) was heated at 100° C. for 6 h. Aqueous potassium fluoride solution (4 M, 120 mL) and EtOAc (200 mL) were added and the resulting mixture was stirred overnight. The mixture was then filtered through Celite and the layers were separated. The organic layer was washed with water and then concentrated under reduced pressure. The residue was purified by silica gel flash chromatography (0-8% MeOH in DCM) to give the title compound (11.8 g, 66% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08816088B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-72744b615cf0448e9207f835072a0e58 |
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| Source note | uspto-grants-2014_08 |
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