HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898490Generated: October 30, 2026
Isopropenyl acetate → Methyl [3-(2-oxopropyl)phenyl]acetate
https://huagongshe.com/reaction/898490
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropenyl acetate | HCID 7916 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| 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 | — |
| Solvent | Potassium Fluoride | HCID 522689 | — |
| Product | Methyl [3-(2-oxopropyl)phenyl]acetate | HCID 21035403 | — |
Reaction Steps
Tributyltin methoxide (28.3 ml, 98 mmol), methyl (3-bromophenyl)acetate (WO 95/27692, pg. 16, e.g. 5a) (15.0 g, 65.0 mmol), isopropenyl acetate (10.8 ml, 98.0 mmol), palladium(II)acetate (750 mg, 3.30 mmol) and tri-ortho-tolylphosphine (2.0 g, 6.5 mmol) were stirred together in toluene (75 ml) at 100° C. under nitrogen for 5 hours. After cooling the reaction was diluted with ethyl acetate (150 ml) and 4M aqueous potassium fluoride solution (90 ml) and stirred for 15 minutes. The mixture was filtered through Arbocel® and the organic phase separated and concentrated in vacuo. The residue was purified column chromatography on silica gel eluting with diethyl ether:pentane (0:100 to 25:75 and then changing to dichloromethane), to yield the title compound as a pale yellow oil, 12.6 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07351742B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-10a691ca20304f518b71afe79a1cc4ee |
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| Source note | uspto-grants-2008_04 |
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