HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → HCID 18999768, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Desmethylmianserin | HCID 115194 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18999768 | HCID 18999768 | 76% |
Reaction Steps
0.832 g of epichlorohydrin was added to a mixture of 4.5 ml of ethanol and 1.5 g of 1,2,3,4,10,14b-hexahydrodibenzo[c,f]pyrazino[1,2-a]azepine, whilst ice-cooling, and the mixture was stirred at room temperature for 5 hours. At the end of this time, it was concentrated by evaporation under reduced pressure. The residue was subjected to column chromatography through silica gel, using a 1:1 by volume mixture of hexane and ethyl acetate as the eluent, to afford 1.56 g (yield 76%) of the title compound as a colorless foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05362725 |
| Source dataset | uspto-grants-1994_11 |
| ORD ID | ord-dc4a03b2d1614993b1ed445b8979256f |
| Source note | uspto-grants-1994_11 |