Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dipropylamine | HCID 8902 | — |
| Reactant | HCID 13306088 | HCID 13306088 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 13343516 | HCID 13343516 | — |
Reaction Steps
2.02 g (0.02 mol) of N,N-dipropylamine and 2.56 g (0.01 mol) of 3-methyl-6-(2-bromoethyl)-benzoxazolinone, dissolved beforehand in 30 cm3 of dioxane, were introduced into a 100 cm3 flask with a ground glass neck, fitted with a reflux condenser, and the mixture was then heated under reflux for seventy-two hours, with stirring. After cooling, the reaction mixture was filtered and the filtrate was then evaporated in a water-bath, in vacuo. The residue was then taken up in 30 cm3 of diethylether, the solution was filtered, the filtrate was washed with water and dried over calcium chloride, and a stream of hydrogen chloride was then bubbled. The precipitate formed was filtered off and then recrystallised from ethylacetate, and this gave 2.23 g of the title compound, in the form of the hydrochloride, having a melting point of 150°-152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04558060 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-89a00e9b52f64ef49edd7756475c9bd5 |
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| Source note | uspto-grants-1985_12 |
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