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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603622Generated: November 1, 2026

Water → N-[3-bromo-5-(4-nitrophenylsulphanyl)-phenyl]-N-methylacetamide

https://huagongshe.com/reaction/1603622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-[3-[2-(phenylsulphonyl)-diazenyl]-5-bromophenyl]-N-methylacetamideHCID 19605539—
Reactant4Nitrothiophenol potassium saltHCID 70002681—
SolventDimethyl SulfoxideHCID 679—
ProductN-[3-bromo-5-(4-nitrophenylsulphanyl)-phenyl]-N-methylacetamideHCID 19605546103.5%

Reaction Conditions

Temperature40 °C

Reaction Steps

0.22 g (0.00055 mol) of N-[3-[2-(phenylsulphonyl)-diazenyl]-5-bromophenyl]-N-methylacetamide was dissolved in 15 ml of dimethyl sulphoxide, treated with 0.185 g (0.000825 mol) of 4-nitrothiophenol potassium salt and stirred at 40° C. for 18 hrs. The reaction mixture was poured into 300 ml of water, extracted with diethyl ether, the organic phase was washed with water and sat. sodium chloride solution, dried over MgSO4, filtered and the filtrate was freed from solvent. The residue was chromatographed on silica gel with 1% MeOH in dichloromethane. There was obtained 0.217 g (100%) of N-[3-bromo-5-(4-nitrophenylsulphanyl)-phenyl]-N-methylacetamide as a yellow oil. MS (EI): me/e=382, 380 (C15H13BrN2O3S+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990105
Source datasetuspto-grants-1999_11
ORD IDord-c4805e378a8f4743a97e08d34da669b8
Source noteuspto-grants-1999_11