HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 10513515, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2,4-Dichlorophenylacetonitrile | HCID 80566 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 10513515 | HCID 10513515 | — |
Reaction Steps
A solution of 2,4-dichlorophenylacetonitrile (30.00 gms , 161 mmol) (Aldrich) in dry ethyl acetate (36 ml) was added dropwise to an ethanolic solution of sodium ethoxide, prepared in situ from sodium metal (4.90 g , 213 mmol) and dry ethanol (60 ml). This reaction mixture was refluxed for two hours, allowed to stand overnight at room temperature and the ethanol was evaporated. The yellow solid obtained was dissolved in water and the resulting solution was extracted twice with ether. The aqueous layer was chilled and acidified with hydrochloric acid. The crude product was extracted with ether to give 23.31 g of white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05597827 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-3ddfa42e5cfe4171937a64fc58642219 |
| Source note | uspto-grants-1997_01 |