HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → N-[4-(1-allyloxyiminoethyl)phenyl]-N'-isopropoxycarbonylmethylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | N-[4-(1-hydroxyiminoethyl)phenyl]-N'-isopropoxycarbonylmethylurea | HCID 72742602 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[4-(1-allyloxyiminoethyl)phenyl]-N'-isopropoxycarbonylmethylurea | HCID 54128761 | — |
Reaction Steps
A solution of the N-[4-(1-hydroxyiminoethyl)phenyl]-N'-isopropoxycarbonylmethylurea in 25% methanolic sodium methoxide (1.0 equivalent) is treated at room temperature with 1.1 equivalent of allyl 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-allyloxyiminoethyl)phenyl]-N'-isopropoxycarbonylmethylurea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04977272 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-ca254232c13e4cf6a5976595cec640d0 |
| Source note | uspto-grants-1990_12 |