HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrylonitrile → 7-(phenylmethoxy)-2H-1-benzopyran-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Dabco | HCID 9237 | — |
| Reactant | 4-Benzyloxy-2-hydroxybenzaldehyde | HCID 561235 | — |
| Product | 7-(phenylmethoxy)-2H-1-benzopyran-3-carbonitrile | HCID 14329758 | 45.7% |
Reaction Steps
A mixture of 1.14 g of 4-benzyloxy-2-hydroxybenzaldehyde, 0.125 g of 1,4-diazabicyclo[2,2,2]octane and 0.65 g of acrylonitrile was stirred and heated at 80°-85° C., under argon, for 2 hours. After removal of the solvent, the residual product was dissolved in tetrahydrofuran-ether(1:1), washed with 1N-sodium hydroxide, water, dried, and the solvents evaporated in vacuo. The crude material (1.10 g) was purified by column chromatography on silica gel to afford 0.6 g (45.7%) of 7-(phenylmethoxy)-2H-1-benzopyran-3-carbonitrile, as a colorless solid mp 95°-98° C. (from ethyl acetatehexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04785017 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-bcdc5da70e454db4af5f3632e112fd17 |
| Source note | uspto-grants-1988_11 |