HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → 4-(Methanesulfonylamino)benzenebutanol methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-(4-Aminophenyl)butan-1-OL | HCID 15006226 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-(Methanesulfonylamino)benzenebutanol methanesulfonate | HCID 54525898 | — |
Reaction Conditions
| Temperature | -10 °C |
|---|
Reaction Steps
9.25 g (0.056 mole) 4-aminobenzenebutanol is dissolved in 100 ml pyridine and the solution is cooled to ca. -10° C. 17.33 ml (25.65 g) (0.244 mole) methanesulfonyl chloride is added dropwise with vigorous stirring at a rate such that the reaction temperature does not rise beyond -5° C. After all methanesulfonyl chloride is added, the reaction mixture is left in the freezer for two days. The reaction mixture is poured onto 300 ml ice water and extracted with 3×200 ml methylene chloride. The combined organic layers are washed with 1 liter cold 5% HCl in 3 portions. The organic layer is dried over sodium sulfate, filtered, and stripped. The residue is crystallized from ethyl acetate/ether to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04613609 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-7231b67d07974c6d9ed1d9df13df13fe |
| Source note | uspto-grants-1986_09 |