HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380339Generated: October 31, 2026
Methanesulfonyl chloride → 4-(Methanesulfonylamino)benzenebutanol methanesulfonate
https://huagongshe.com/reaction/1380339
Participants
| Role | Name | HCID | Charge |
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| 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 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 |
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| Patent number | US04581370 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-d0df65651268455d9a7aa0f9b89b5d07 |
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| Source note | uspto-grants-1986_04 |
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