HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 21450746, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 7,7-Diphenyl-1,4-oxazepane | HCID 20326629 | — |
| Product | HCID 21450746 | HCID 21450746 | — |
Reaction Steps
To the stirred solution of 5.06 g of 7,7-diphenyl-hexahydro-1,4-oxazepine in 50 ml of methylene chloride, 2.6 g of allyl bromide are added, followed by 40 ml of 10% aqueous sodium bicarbonate and the mixture is stirred for 24 hours at room temperature. The organic layer is separated, washed with water, dried, filtered and evaporated. The residue is taken up in acetone, the solution acidified with hydrogen chloride in acetone and diluted with diethyl ether, to yield the 4-allyl-7,7-diphenyl-hexahydro-1,4-oxazepine hydrochloride melting at 246° to 247°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04010166 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-66ea9860a23943669ddd612cac5b6dc2 |
| Source note | uspto-grants-1977_03 |