HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Butene, 1-bromo- → N-[4-(1-crotyloxyiminoethyl)phenyl]-N'-ethoxycarbonylmethylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Butene, 1-bromo- | HCID 122414 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | N-[4-(1-hydroxyiminoethyl)phenyl]-N'-ethoxycarbonylmethylurea | HCID 72742601 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[4-(1-crotyloxyiminoethyl)phenyl]-N'-ethoxycarbonylmethylurea | HCID 53692223 | — |
Reaction Steps
A solution of the N-[4-(1-hydroxyiminoethyl)phenyl]-N'-ethoxycarbonylmethylurea in 25% methanolic sodium methoxide (1.0 equivalent) is treated at room temperature with 1.1 equivalent of crotyl bromide. The reaction mixture is stirred until the temperature falls to about 20° C. The reaction mixture is then poured into cold water and extracted with diethyl ether. The ether solution is dried over MgSO4 and filtered, and the solvent is removed by rotary evaporator to yield the product N-[4-(1-crotyloxyiminoethyl)phenyl]-N'-ethoxycarbonylmethylurea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04977272 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-0c2aab5e3a6b48bb9e6c65dd0b2eeb7b |
| Source note | uspto-grants-1990_12 |