HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-Ethyl-3-(3-methoxyphenyl)azepan-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Hexahydro-3-(3-methoxyphenyl)-2H-azepin-2-one | HCID 12875111 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Ethyl-3-(3-methoxyphenyl)azepan-2-one | HCID 2815455 | — |
Reaction Steps
Hexahydro-3-(3-methoxyphenyl)-2H-azepin-2-one (2.19 g) in dry tetrahydrofuran was added to a stirred solution of lithium diisopropylamide (from butyllithium 1.4 molar 15.7 ml, and diisopropylamine 3.15 ml) under nitrogen at 0° C. Ethyl bromide (1 ml) was added in one portion and the reaction allowed to warm up to room temperature. After two hours the reaction was poured into 2 M HCl, the organic layer separated and the aqueous layer extracted with chloroform. The combined organic layers were dried over magnesium sulphate, filtered and evaporated to an oil which was crystallised from ethyl acetate giving 1.68 g of the title compound m.p. 85°-7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04197241 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-78cda70d79e94ff88c60ae155e2e86eb |
| Source note | uspto-grants-1980_04 |