HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178513225, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 6-Bromonaphthalene-2-carbonitrile | HCID 14662115 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178513225 | HCID 178513225 | — |
Reaction Steps
2.48 g hydroxylamine-hydrochloride and 5.68 ml triethylamine are added to 4.10 g of 6-bromo-2-cyano-naphthalene in 100 ml of ethanol and the reaction mixture is refluxed for four hours. After cooling to ambient temperature the solvent is distilled off in vacuo using the rotary evaporator and the flask residue is divided between water and ethyl acetate. The aqueous phase is extracted with ethyl acetate and the combined organic phases are dried on magnesium sulphate and evaporated down.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163911B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-de8976d12e9940d2bc603ab462d1e8e3 |
| Source note | uspto-grants-2012_04 |