HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-(4-Bromophenyl)-1-(methanesulphonyl)piperidin-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-(4-Bromophenyl)-4-hydroxypiperidine | HCID 93911 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Bromophenyl)-1-(methanesulphonyl)piperidin-4-ol | HCID 18723205 | — |
Reaction Steps
1 g of 4-(4-bromophenyl)piperidin-4-ol is placed in 20 ml of dichloromethane. 0.65 ml of triethylamine and then 0.33 ml of methanesulphonyl chloride are added. The reaction mixture is stirred at ambient temperature for 2 h. It is washed with water and then with a saturated aqueous sodium chloride solution. The organic phase is dried over sodium sulphate and then evaporated under reduced pressure. The crude product obtained is chromatographed on silica gel, elution being carried out with a dichloromethane/methanol (99/1) solvent mixture. 1.1 g of 4-(4-bromophenyl)-1-(methanesulphonyl)piperidin-4-ol are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08530657B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-912b160d0d294e57b5d2e395040ec0ab |
| Source note | uspto-grants-2013_09 |