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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106742Generated: October 31, 2026

Methanol → N-[2-methyl-3(2-oxo-ethyl)-phenyl]-methanesulfonamide

https://huagongshe.com/reaction/1106742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN-(3-cyanomethyl-2-methyl-phenyl)-methanesulfonamideHCID 18789726—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTetrahydrofuranHCID 8028—
ProductN-[2-methyl-3(2-oxo-ethyl)-phenyl]-methanesulfonamideHCID 18789617—

Reaction Conditions

Temperature5 °C

Reaction Steps

N-(3-cyanomethyl-2-methyl-phenyl)-methanesulfonamide (3.75 g) was dissolved in 50 ml of dry tetrahydrofuran and cooled in an ice bath under an atmosphere of nitrogen. To this mixture was added 67 ml of 1M diisobutylaluminum hydride (DIBAL) in tetrahydrofuran. The mixture was stirred at 5° C. for 75 minutes. Excess reagent was decomposed with methanol and the solvent was evaporated. The residue was treated with EtOAc, washed with cold 1M hydrochloric acid, washed with brine and dried, and the solvent was evaporated. The residue was purified by silica gel chromatography eluting with methanol:dichloromethane (5:95), giving 1.1 g of N-[2-methyl-3(2-oxo-ethyl)-phenyl]-methanesulfonamide as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057349
Source datasetuspto-grants-2000_05
ORD IDord-6df12b9f6c0145ffbec102d74444369d
Source noteuspto-grants-2000_05