HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → Ethyl-alpha-bromo-p-cyanophenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Ethyl 2-(4-cyanophenyl)acetate | HCID 279718 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | Ethyl-alpha-bromo-p-cyanophenylacetate | HCID 19930427 | — |
Reaction Steps
A solution of 1,9 g of ethyl p-cyanophenylacetate in 50 ml of diglyme is added to a slurry of 0.48 g of sodium hydride (50% oil dispersion) in 10 ml of diglyme. The reaction mixture is stirred at room temperature for 2 h, cooled to 0° and 1.75 g of N-bromosuccinimide is added portionwise. The solvent is evaporated under high vacuum and the residue is chromatographed on 50 g of silica with ether to yield ethyl-α-bromo-p-cyanophenylacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04889861 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-aeb8b12e44654cc8a1acd224b18d54f9 |
| Source note | uspto-grants-1989_12 |