HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidin-4-ol → 4-((4-Hydroxypiperidin-1-yl)sulfonyl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Formylbenzene-1-sulfonyl chloride | HCID 2759210 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-((4-Hydroxypiperidin-1-yl)sulfonyl)benzaldehyde | HCID 86624855 | — |
Reaction Steps
To 4-formyl-benzenesulfonyl chloride (1.0 g) in DCM (10 mL) was added 4-hydroxypiperidine (0.984 g), followed by NaHCO3 (10 mL, aq sat'd) and the mixture stirred for 2 h at RT. The aqueous layer was washed with DCM (2×25 mL), and the combined organic portions washed with brine, dried over Na2SO4, filtered, and the solvent removed under reduced pressure to provide 4-(4-hydroxypiperidine-1-sulfonyl)benzaldehyde. The product was purified on anhydrous silica (10% MeOH/DCM). M+H 269.9
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08163906B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-d4f28b959ab341d69b62e4980688dec1 |
| Source note | uspto-grants-2012_04 |