Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyl acrylate | HCID 15458 | — |
| Reactant | HCID 14888723 | HCID 14888723 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14888724 | HCID 14888724 | 60% |
Reaction Steps
A solution of benzyl 2-(4-bromophenyl)acetate (33.5 g. 0.11 mol), t-butyl acrylate (31.6 mL, 0.22 mol) and triethylamine (85 mL. 0.64 mol) in DMF (1000 mL) was deoxygenated with argon, whereupon bis(triphenylphosphine)palladium dichloride (5.1 g. 8.3 mmol) was added. After heating at 75° C. for 12 hours the solvent was removed in vacuo providing a brown residue that was purified by chromatography on silica gel using a mixture of hexanes and ethyl acetate (9:1) to give benzyl (E)-2-[4-[3-(1,1-dimethylethoxy)-3-oxo-1-propenyl]phenyl]acetate as a pale yellow oil (23.3 g. 0.07 mol) in 60% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05296608 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-d4728514b09c492aabb2e20109d39940 |
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| Source note | uspto-grants-1994_03 |
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