HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 86743382, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 86743383 | HCID 86743383 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86743382 | HCID 86743382 | — |
Reaction Steps
A solution of 0.01 mol of 3-[4-(hydroxyiminomethyl)phenyl]-5-methoxycarbonylhydantoin in diethyl ether is treated with 0.01 mol of sodium hydride. After hydrogen evolutionstops, 0.011 mol of allyl bromide is added. The reaction mixture is stirredfor 2 hours. The reaction mixture is then poured into cold water, the layers are separated, and the aqueous layer is extracted with diethyl ether. The combined ether solutions are dried over MgSO4 and filtered, and the solvent is removed by rotary evaporator to yield 3-[4-(allyloxyiminomethyl)phenyl]-5-methoxycarbonylhydantoin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04868061 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-75b53097b7324d6bb93b2c41539b3be7 |
| Source note | uspto-grants-1989_09 |