HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexene → Tetraethyl aminomethylenediphosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexene | HCID 8079 | — |
| Reactant | HCID 10961905 | HCID 10961905 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Tetraethyl aminomethylenediphosphonate | HCID 2773808 | — |
Reaction Steps
Compound 143 (2.00 g, 4.14 mmol) was dissolved in EtOH (40 mL). To this solution was added palladium on carbon (10%, 1.5 g) and cyclohexene (2.5 mL, 24.7 mmol). The reaction mixture was refluxed under argon for 15 hours, filtered through celite and evaporated to give 144 as a slightly impure pale yellow oil (1.50 g, 119%), which was used directly in the next step without further purification. 1H NMR (400 MHz, CDCl3) δ 1.35 (t, J=7.0, 12H), 3.58 (t, J=20.3, 1H), 3.65-3.90 (br s, 2H), 4.20-4.28 (m, 8H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524691B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-e08e3f0493e740448f025f50c28f4ad2 |
| Source note | uspto-grants-2013_09 |