HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl methylphosphonate → HCID 22914177, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienal | HCID 5280598 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22914177 | HCID 22914177 | — |
Reaction Steps
n-Butyllithium (0.698 ml of a 2.5M solution in hexanes, 1.75 mmol) was added to a stirred solution of dimethyl methylphosphonate (0.189 ml, 1.75 mmol) in THF (4 ml), under argon at -78° C. The resulting colorless solution was stirred at this temperature for 20 min. Farnesal (350 mg, 1.59 mmol) in THF (4 ml) was added over 5 min and the resulting mixture stirred a further 30 min and then treated with saturated sodium bicarbonate solution (5 ml) and allowed to warm to r.t. The THF was evaporated in vacuo and the aqueous extracted twice with ethylacetate, washed with brine, dried (MgSO4) and concentrated in vacuo. The residue was chromatographed on silica gel eluted with ethylacetate to afford the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05298655 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-bcbaf12a61eb494ba327df932afa2d37 |
| Source note | uspto-grants-1994_03 |