HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 21094277, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Reactant | (3-Methoxyphenyl)acetonitrile | HCID 88310 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21094277 | HCID 21094277 | — |
Reaction Steps
Two grams of (3-methoxyphenyl)acetonitrile and 1.5 ml of ethyl 4-bromobutyrate are dissolved in 50 ml of dimethylformamide at 0° C. Six hundred milligrams of 60% sodium hydride (600 mg; 15 mmol) are progressively added to the solution. The reaction mixture is stirred at ambient temperature for 4 hours, taken up in 100 ml of acidic water and extracted with ether. The organic phase is then dried over magnesium sulphate, filtered and evaporated under reduced pressure. The oil obtained is purified on a column (eluant:ether/cyclohexane 4/6) to yield the title product in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07214689B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-1f1659075bbf467abb49920bdc648e12 |
| Source note | uspto-grants-2007_05 |