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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72369Generated: October 25, 2026

Ammonium Acetate → N-(tert-Butyl)-2-amino-2-(4-fluorophenyl)ethanesulfonamide

https://huagongshe.com/reaction/72369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantN-(tert-Butyl)-2-(4-fluorophenyl)-2-oxoethanesulfonamideHCID 68288463—
SolventMethanolHCID 887—
ProductN-(tert-Butyl)-2-amino-2-(4-fluorophenyl)ethanesulfonamideHCID 68287917—

Reaction Steps

A solution of 0.66 g of N-(tert-butyl)-2-(4-fluorophenyl)-2-oxoethanesulfonamide, 1.85 g of ammonium acetate and 0.17 g of sodium cyanoborohydride in 12 ml of methanol was stirred at 60° C. for 17 hours. After the removal of the solvent under reduced pressure, the residue was taken up in 50 ml of ethyl acetate and washed twice with 30 ml of 0.5 N aqueous sodium hydroxide solution and 30 ml of saturated aqueous sodium chloride solution. The organic phase was dried over MgSO4 and concentrated by rotary evaporation. The crude product was subjected to a chiral separation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828994B2
Source datasetuspto-grants-2014_09
ORD IDord-862b77b448334435a0c2e674fe13fedc
Source noteuspto-grants-2014_09