HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 1-(2-(2,3,4,5-Tetrahydro-7-cyano-1-benzoxepin-5-yl)ethyl)-4-(3,4-dimethoxyphenyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(2,3,4,5-Tetrahydro-7-cyano-1-benzoxepin-5-yl)ethyl bromide | HCID 18986519 | — |
| Reactant | 4-(3,4-Dimethoxyphenyl)piperidine hydrochloride | HCID 18986577 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 1-(2-(2,3,4,5-Tetrahydro-7-cyano-1-benzoxepin-5-yl)ethyl)-4-(3,4-dimethoxyphenyl)piperidine | HCID 18986523 | — |
Reaction Steps
3.6 g of 2-(2,3,4,5-tetrahydro-7-cyano-1-benzoxepin-5-yl)ethyl bromide [obtainable starting from 2,3,4,5-tetrahydro-7-cyano-1-benzoexpin-5-one [sic] by reaction with triphenylethylphosphinium bromide, subsequent bromination of the product in the allyl position and reduction of the isolated double bond with diisobutyl-aluminiumhydride (DIBAH)], 1 equivalent of 4-(3,4-dimethoxyphenyl)piperidine hydrochloride, 3.8 g of K2CO3 and 2.1 g of KI are dissolved in 120 ml of ethyl methyl ketone and the mixture is boiled for 3 hours. Customary working up gives 1-(2-(2,3,4,5-tetrahydro-7-cyano-1-benzoxepin-5-yl)ethyl)-4-(3,4-dimethoxyphenyl)piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05495022 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-af3eb4b01e1c4d9da7abb7616e6fe4d6 |
| Source note | uspto-grants-1996_02 |