Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Methylpyridine | HCID 7970 | — |
| Reactant | HCID 58338516 | HCID 58338516 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 24742482 | HCID 24742482 | — |
Reaction Steps
cis-cis-1,12-Dibromo-dodeca-5,7-diene was added to a solution of 3-picoline (3 mmol) in acetonitrile and the solution refluxed for 24 hours. The acetonitrile was removed in vacuum and the resulting residue was partitioned between ether and water. The aqueous layer was washed extensively with ether until no picoline left in the aqueous layer. The resulting aqueous solution of the product was lyophilized to yield the pure product. (76%). 1HNMR (300 MHz, D2O, ppm) 8.50 (s, 2H), 8.44 (d, J=6.3, 2H), 8.16 (d, J=7.8, 2H), 7.74 (dd, J=7.8, J=6.3, 2H), 6.15-6.18 (m, 2H), 5.38-5.38 (m, 2H), 4.38 (t, J=5.7, 4H), 2.35 (s, 6H), 2.06 (q, J=7.5, 4H), 1.83 (p, J=7.5, 4H), 1.25 (p, J=7.5, 4H). 13CNMR, 145.99, 143.71, 141.30, 139.95, 132.19, 127.46, 124.06, 61.69, 30.27, 26.35, 25.44, 17.93.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08178678B2 |
|---|
| Source dataset | uspto-grants-2012_05 |
|---|
| ORD ID | ord-18dcfafb82754b928f68a7c2f6e12d85 |
|---|
| Source note | uspto-grants-2012_05 |
|---|