HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-(1-(4-oxocyclohexyl)propyl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 58562472 | HCID 58562472 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(1-(4-oxocyclohexyl)propyl)methanesulfonamide | HCID 58562881 | — |
Reaction Steps
A solution of N-(1-1,4-dioxaspiro[4.5]decan-8-ylpropyl)methanesulfonamide (as prepared in the previous step, 38 mg, 0.14 mmol, 1.00 equiv) in CH3CN (5 mL) and HCl (2M, 1 mL) was stirred for 2 h at room temperature. The resulting mixture was concentrated under vacuum. The residue was diluted with 10 mL of aq. sodium bicarbonate (1M). The resulting solution was extracted with 2×20 mL of dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate and concentrated under vacuum to give the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09062048B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-d213c9948f5d4cd7b28144831f60bda6 |
| Source note | uspto-grants-2015_06 |