HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 18946314, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | 4-Aminophenylacetonitrile | HCID 77000 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18946314 | HCID 18946314 | 51% |
Reaction Steps
A mixture of 4-aminobenzylcyanide (10 g, 75.7 mmol), epichlorohydrine (7.9 ml, 9.25 g, 100 mmol), ethanol (15 ml) and water (10 ml) was heated under reflux for 2 hours. After cooling the reaction mixture was poured into 100 ml of water and extracted with ether (3×50 ml). The organic extracts were combined and stirred with 50 ml of 10N NaOH at room temperature for 3 hours. The organic layer was separated, washed with water until neutral, dried over MgSO4 and concentrated. The residue was chromatographed over a silica gel column eluting with a 3:1 mixture of benzene and ethyl acetate to afford 7.24 g of the title compound as an oil, yield: 51.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05380724 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-60aecbedda6d456b8a0875cd91e93612 |
| Source note | uspto-grants-1995_01 |