HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Cinnamate → Methyl 4-methylene-2-phenylcyclopentanecarboxylate, trans-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Cinnamate | HCID 637520 | — |
| Reactant | 2-(Trimethylsilylmethyl)allyl acetate | HCID 4428347 | — |
| Catalyst | 1,2-Bis(diphenylphosphino)ethane | HCID 74267 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 4-methylene-2-phenylcyclopentanecarboxylate, trans- | HCID 12537224 | 92.5% |
Reaction Steps
A mixture of methyl trans-cinnamate (5.0 g, 31 mmol), tetrakis(triphenylphosphine) palladium(0) (2.6 g, 2.3 mmol), 1,2-bis(diphenylphosphino)ethane (0.70 g, 1.8 mmol) and 2-((trimethylsilyl)methyl)-2-propen-1-yl acetate (6.90 g, 37 mmol) in THF (60 mL) under argon was heated to reflux for 4 h. An additional aliquot of 2-((trimethylsilyl)methyl)-2-propen-1-yl acetate (3.40 g) was added and the reaction was continued for another 16 h. The volatiles were then removed in vacuo and the residue was purified by FC (10% ethyl acetate in hexanes) to afford the title compound (6.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06358979B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-976102adcbff4072bff35b8fcd878b13 |
| Source note | uspto-grants-2002_03 |