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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72347Generated: October 26, 2026

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

https://huagongshe.com/reaction/72347

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 68287917105.7%

Reaction Steps

A solution of N-(tert-butyl)-2-(4-fluorophenyl)-2-oxoethanesulfonamide (657 mg), ammonium acetate (1.85 g) and sodium cyanoborohydride (166 mg) was stirred in methanol (12 ml) at 60° C. for 17 hours. The reaction solution was concentrated by rotary evaporation and the residue was taken up in ethyl acetate (50 ml). Then it was washed with 0.5 N aqueous sodium hydroxide solution (50 ml) and with saturated sodium chloride solution (50 ml), and the organic phase was dried over MgSO4, filtered and concentrated under reduced pressure. This gave the product (697 mg) with a molecular weight of 274.3 g/mol (C12H19FN2O2S), MS (ESI): m/e=275 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828995B2
Source datasetuspto-grants-2014_09
ORD IDord-e6e383aa11d742978b08a562cc141a0b
Source noteuspto-grants-2014_09