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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65228Generated: October 30, 2026

Methanesulfonyl chloride → 4-(Methanesulfonylamino)benzenebutanol methanesulfonate

https://huagongshe.com/reaction/65228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-(4-Aminophenyl)butan-1-OLHCID 15006226—
SolventPyridineHCID 1049—
Product4-(Methanesulfonylamino)benzenebutanol methanesulfonateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04613609
Source datasetuspto-grants-1986_09
ORD IDord-7231b67d07974c6d9ed1d9df13df13fe
Source noteuspto-grants-1986_09