HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 15860308, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Diethyl (cyanomethyl)phosphonate | HCID 75676 | — |
| Reactant | 2-Fluoro-5-methoxybenzaldehyde | HCID 2734872 | — |
| Reactant | HCID 70274102 | HCID 70274102 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15860308 | HCID 15860308 | — |
Reaction Steps
(trans)-3-(2-Fluoro-5-methoxyphenyl)-2-propenenitrile: To a suspension of NaH (6.90 g, 60% dispersion in mineral oil, 173 mmol) in THF (500 mL) at 0° C. was added diethyl cyanomethylphosphonate (30.10 g, 170 mmol) dropwise. This was followed by the dropwise addition of a solution of 2-fluoro-5-methoxybenzaldehyde (24.5 g, 159 mmol) in THF (50 mL). The resulting suspension was allowed to warm to ambient temperature. After 18 h, H2O (200 mL) was added and the solution was extracted with EtOAc. The organics were combined, washed with brine, dried over MgSO4, and concentrated to afford a white waxy solid. The material was then purified by Kugelrohr distillation to give the title compound, 24.3 g (86%): mp 56°-57° C.;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753709 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-d0b61c9fe71f453085701ac244dc1921 |
| Source note | uspto-grants-1998_05 |