HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aluminum(III) Chloride → 7-Hydroxy-4-methyl-6-(1-piperidinesulfonyl)-1-indanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Piperidine-1-sulfonyl chloride | HCID 11298344 | — |
| Reactant | 7-Hydroxy-4-methyl-1-indanone | HCID 12436244 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 7-Hydroxy-4-methyl-6-(1-piperidinesulfonyl)-1-indanone | HCID 13604156 | 32.5% |
Reaction Steps
Into a solution of 2 g of 7-hydroxy-4-methyl-1-indanone in 10 ml of dichloroethane was added 2.27 g of 1-piperidine sulfonyl chloride. Then 10 g of anhydrous aluminum chloride was gradually added to the mixture and stirred, and the reaction mixture was refluxed by heating for 8 hours. The reaction mixture was extracted with 200 ml of chloroform, washed with water, then the chloroform was removed by evaporation under a reduced pressure. The residue was purified by means of a silica gel column chromatography (eluent: chloroform), and recrystallized from ethanol to obtain 1.24 g of 7-hydroxy-4-methyl-6-(1-piperidinesulfonyl)-1-indanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04792628 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-44f3a295932047cc86a976dc939984c6 |
| Source note | uspto-grants-1988_12 |