Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 7-Hydroxyflavone | HCID 5281894 | — |
| Reactant | 2-[3-(Oxiran-2-yl)propoxy]oxane | HCID 19835341 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 14626328 | HCID 14626328 | — |
Reaction Steps
A solid mixture of 7-hydroxyflavone (32.0 g, 0.134 mol), piperidine (0.5 ml), and 2-(4,5-epoxypent-1-oxy)tetrahydropyran (50 g, 0.268 mol) was stirred and heated under nitrogen at 100° C. for 14 hours; it became a stirrable mixture after 6 hours heating at 100° C. The cooled reaction mixture was purified through a pad of silica gel eluting with CH2Cl2 initially and then CH2Cl2 --EtOAc (1:1). The resulting solid was stirred with ether and filtered, giving 43.9 g (77% crude yield) of an off-white solid; pure white crystals, mp 110°-112° C., were obtained from recrystallization from toluene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04889941 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-6b3b9652ea02441f9dd6f743128730bf |
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| Source note | uspto-grants-1989_12 |
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