HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Octanol → HCID 12642364, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Octanol | HCID 957 | — |
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 12642364 | HCID 12642364 | — |
Reaction Steps
To a suspension of 15.60 g sodium hydride (60%) in 200 ml of 1,2-dimethoxyethane, 50.79 g of 1-octanol was dropped in. The mixture was stirred for 45 minutes at room temperature. Then, 46.76 g of bromoacetonitrile was dropped in. The reaction mixture was refluxed for 2 hours, quenched with water, filtered, and diluted with brine. After extraction with ether, the organic layer was washed with brine and water, dried, filtered, and evaporated to dryness. The resulting dark oil was purified by distillation to yield a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06258854B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-b31b1c99fe1341fea777bcf19b67ed90 |
| Source note | uspto-grants-2001_07 |