HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-Cyano-2,3-dihydro-3,3-dimethyl-2-ethoxybenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Hydroxy-3,3-dimethyl-2,3-dihydrobenzofuran-5-carbonitrile | HCID 20536200 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Cyano-2,3-dihydro-3,3-dimethyl-2-ethoxybenzofuran | HCID 20536184 | — |
Reaction Steps
The product of stage (b) (32.2 g) was boiled under reflux in ethanol (200 ml) containing sulphuric acid (7 drops), for 2 hours. The solution was cooled, neutralised with triethylamine and reduced to half volume under vacuum. Addition to water and isolation through diethyl ether gave 34.4 g of crude title product as a yellow oil. This was dissolved in petroleum ether bp 40°-60° C. containing 5% diethyl ether, then filtered through a bed of aluminium oxide followed by elution with the same solvent mixture. This yielded 30.5 g of the pure product as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04263037 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-74cb74986bde4f89a0e26dcf6520d703 |
| Source note | uspto-grants-1981_04 |