HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Octanol → HCID 53635237, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Octanol | HCID 957 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 53777893 | HCID 53777893 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 53635237 | HCID 53635237 | — |
Reaction Steps
A suspension of 2.1 g (50 millimols) of sodium hydride (in oil) is added in small amounts to 6.5 g (50 millimols) of octan-1-ol in 100 ml of toluene, whilst stirring. When the evolution of hydrogen has ended, 16.6 g (50 millimols) of 3-(p-bromomethylbenzylidene)-camphor are added in portions, and the mixture is then heated under reflux for 3 hours. After adding water, the toluene phase is decanted, dried and concentrated to dryness. The residual syrup is distilled under reduced pressure. 8.8 g of a yellow liquid, which boils at 240° under a pressure of 0.1 mm Hg, are thus collected.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04421739 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-dc9011886d4a44bf80750b718a241b3f |
| Source note | uspto-grants-1983_12 |