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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405466Generated: November 1, 2026

Methanol → 4'-bromo-N-methyl-2'-aminobenzanilide

https://huagongshe.com/reaction/2405466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium DithioniteHCID 24489—
ReactantSodium BicarbonateHCID 516892—
Reactant4'-bromo-N-methyl-2'-nitrobenzanilideHCID 23094078—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product4'-bromo-N-methyl-2'-aminobenzanilideHCID 2309407391.3%

Reaction Steps

9.5 g (28 mmol) of 4′-bromo-N-methyl-2′-nitrobenzanilide was dissolved in 100 mL of tetrahydrofuran. A solution of 25 g (142 mmol) of sodium hydrosulfite in 90 mL of water was added to the solution while stirring the solution at room temperature in an argon atmosphere. After the addition of 10 mL of methanol, the mixture was stirred for 3 hours. After the addition of 100 mL of ethyl acetate, a solution of 12 g (142 mmol) of sodium hydrogencarbonate in 125 mL of water was added to the mixture. After stirring the mixture at room temperature for 1 hour, the mixture was extracted with ethyl acetate. After removing the aqueous phase, the organic phase was washed with a 10% potassium carbonate aqueous solution and a saturated sodium chloride solution, and dried over magnesium sulfate. After filtering the organic phase, the solvent was evaporated under reduced pressure to obtain 7.8 g of 4′-bromo-N-methyl-2′-aminobenzanilide as a white solid (yield: 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08803420B2
Source datasetuspto-grants-2014_08
ORD IDord-8fb2cc6249a5481e92ebc8c20b10c827
Source noteuspto-grants-2014_08