HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 3-bromo-6,7,8,9-tetrahydro-5H-10-thia-7-aza-benzo[a]azulene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 3-bromo-5,6,8,9-tetrahydro-10-thia-7-aza-benzo[a]azulen-7-carboxylate | HCID 69079455 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-bromo-6,7,8,9-tetrahydro-5H-10-thia-7-aza-benzo[a]azulene | HCID 67364287 | — |
Reaction Steps
30.0 g (53.5 mmol) KOH in 700 mL EtOH are added to a solution of 19.0 g (53.5 mmol) ethyl 3-bromo-5,6,8,9-tetrahydro-10-thia-7-aza-benzo[a]azulen-7-carboxylate. EtOH is distilled off at normal pressure and the residue is taken up in water. The solution is acidified with HCl. Then it is made basic with NaOH and the aqueous phase is extracted four times with chloroform. The organic phase is dried over Na2SO4 and K2CO3 and the solvent is eliminated i.vac. The purification is carried out by repeated column chromatography on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07452911B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-5d613efc1a91423484a71d7d78ac9e5d |
| Source note | uspto-grants-2008_11 |