HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → HCID 20344789, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | hexahydro-3-(3-methoxyphenyl)-1-methyl-2H-azepin-2-one | HCID 2727906 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 20344789 | HCID 20344789 | — |
Reaction Steps
Lithium diisopropylamide, prepared by adding 15% butyl lithium in hexane (15.7 ml) to diisopropylamine (3.15 ml) at -10° C. under nitrogen, was treated with a solution of hexahydro-3-(3-methoxyphenyl)-1-methyl-2H-azepin-2-one in THF. After 30 minutes, ethyl bromide (1.0 ml) was added. The mixture was allowed to warm to ambient temperature. After a further 2 hours the reaction was quenched with water. The organic layer was evaporated to give an oil that crystallised on scratching. The solid was recrystallised from ethyl acetate to give the title compound (1.68 g) m.p. 85°-87° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04197241 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-11d699669cd74491a00fe9e4f41439f3 |
| Source note | uspto-grants-1980_04 |