HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 10705792, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Fluorobenzyl bromide | HCID 68021 | — |
| Reactant | NSC57392 | HCID 245432 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 10705792 | HCID 10705792 | — |
Reaction Steps
To a stirred suspension of n-hexane-washed sodium hydride (0.94 g, 39.0 mmol, 1.3 eq) there was added a solution of ethoxyethyl 2-oxocyclopentane-carboxylate (4.26 g, 30.0 mmol, 1.0 eq) in DMF (15 ml) at 0° C. The resulting solution was warmed to room temperature and then stirred for 30 min: the solution became orange. After terminal evolution of hydrogen had been confirmed, p-fluorobenzyl bromide (6.80 g, 36.0 m mol, 1.2 eq) was added to the resulting solution at 0° C. The reaction mixture was then warmed to room temperature and stirred overnight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05286737 |
| Source dataset | uspto-grants-1994_02 |
| ORD ID | ord-93a9951843764d85be4c1befc527630f |
| Source note | uspto-grants-1994_02 |