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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848635Generated: October 31, 2026

o-(Methylamino)phenol → 3-bromo-4-chloro-N-(2-hydroxy-phenyl)-N-methyl-benzamide

https://huagongshe.com/reaction/1848635

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-(Methylamino)phenolHCID 69138—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Bromo-4-chlorobenzoyl chlorideHCID 20229730—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3-bromo-4-chloro-N-(2-hydroxy-phenyl)-N-methyl-benzamideHCID 6860311756.3%

Reaction Steps

3-Bromo-4-chloro-benzoyl chloride (Step 2A, 106.9 mmol) in acetonitrile (300 mL) was added dropwise over 30 minutes to a vigorously stirring solution of 2-methylamino-phenol (15.1 g, 122.9 mmol) and NaHCO3 (18.0 g, 213.7 mmol) in acetonitrile (200 mL) and water (200 mL). The mixture was stirred for additional 1 h and then concentrated to remove acetonitrile. The solid was filtered, washed with HCl (1N, 600 mL) and water (500 mL), and dried. The solid was dissolved in dichloromethane (500 mL) and n-butylamine (20 mL) was added. The mixture was stirred at rt for 16 hrs and concentrated. The residue was partially purified via silica gel flash chromatography (eluting with 20% to 35% ethyl acetate in hexane) and then crystallized from hexane/ethyl acetate (75/25) to give 3-bromo-4-chloro-N-(2-hydroxy-phenyl)-N-methyl-benzamide (20.5 g) as a white solid. MS [M+H]+: 339.7/341.8; tR=2.19 min. (method 1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952161B2
Source datasetuspto-grants-2015_02
ORD IDord-e773782549a442a8aa069d0b280a2e2b
Source noteuspto-grants-2015_02