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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24884Generated: October 25, 2026

Bromoacetonitrile → n-Cyanomethyl-n-methylsulphonyl-4-nitroaniline

https://huagongshe.com/reaction/24884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetonitrileHCID 11534—
ReactantN-(4-nitrophenyl)methanesulfonamideHCID 4689022—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
Productn-Cyanomethyl-n-methylsulphonyl-4-nitroanilineHCID 22569517—

Reaction Steps

3.24 g (15 mmol) of N-methylsulphonyl-4-nitroaniline are dissolved in 25 ml of DMSO and a total of 2.0 g (18 mmol) of potassium tert.butoxide are added batchwise. After 1 hour stirring at ambient temperature 2.7 g (23 mmol) of bromoacetonitrile are added dropwise. After 3 hours stirring at ambient temperature the mixture is poured onto ice water and extracted with ethyl acetate. The organic phase is washed with water and the solvent is eliminated in vacuo. The residue thus obtained is recrystallised from ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855710B2
Source datasetuspto-grants-2005_02
ORD IDord-dc456cbe6fbe4898aee71532eb090652
Source noteuspto-grants-2005_02