HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-[(2-Butoxyphenoxy)methyl]oxirane → HCID 23349132, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-[(2-Butoxyphenoxy)methyl]oxirane | HCID 20249276 | — |
| Reactant | HCID 23349122 | HCID 23349122 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23349132 | HCID 23349132 | 74% |
Reaction Steps
4.5 g of 2-n-butoxyphenyl glycidyl ether ##STR27## are heated under reflux together with 5.8 g of N-benzyl-N'-[1,3-dimethyl-2,4-dioxopyrimid-6-yl]ethylenediamine ##STR28## (in 150 ml of ethanol) for 2 hours. The resulting solution is then cooled and concentrated in vacuo. A resinous residue remains. This residue is dissolved in 150 ml of dioxane (without further purification) and then hydrogenated with H2 in the presence of Pd/C at 20° C. for 10 hours. The catalyst is then filtered of; the filtrate is concentrated; and the residue is recrystallized once from toluene. N-[3-(o-Butoxyphenoxy)-2-hydroxypropyl]-N'-[1,3-dimethyl-2,4-dioxopyrimid-6-yl]ethylenediamine of the formula ##STR29## is thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04216314 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-e191f19071ee4374b0d1224343a18eff |
| Source note | uspto-grants-1980_08 |