HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Acrylate → Methyl (E)-3-(6-heptyloxynaphth-2-yl)acrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Acrylate | HCID 7294 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | 6-Bromo-2-heptyloxynaphthalene | HCID 10615713 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Methyl (E)-3-(6-heptyloxynaphth-2-yl)acrylate | HCID 21182539 | — |
Reaction Steps
A mixture of 5.2 g of 6-bromo-2-heptyloxynaphthalene, 25 ml of triethylamine, 4.3 ml of methyl acrylate, 0.072 g of palladium acetate and 0.392 g of tri-o-tolylphosphine is refluxed for 16 hours. The reaction mixture is then cooled and is partitioned between ethyl acetate and water and the organic phase is washed with water, dried over magnesium sulfate, filtered and evaporated down. The residue is chromatographed over 250 g of silica gel using toluene/ethyl acetate (3:1) and then crystallized from toluene. This gives methyl (E)-3-(heptyloxynaphth-2-yl)acrylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06277502B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-66da3151daeb4fe9bf4d1e312a52499b |
| Source note | uspto-grants-2001_08 |