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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513115Generated: October 29, 2026

Dimethylamine → HCID 67505515, compound

https://huagongshe.com/reaction/513115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 67505546HCID 67505546—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 67505515HCID 6750551553%

Reaction Steps

To a solution of N-[4-chloro-2-(2-methyl-benzoyl)-phenyl]-benzamide (5.1 g, 14.6 mmol) and N-bromosuccinimide (2.85 g, 16 mmol) in CCl4 (150 mL) was added 2,2′-azobisisobutylnitrile (0.2 g, 1.5 mmol). The solution was refluxed for 4 h. The solution was then cooled to room temperature, diluted with CH2Cl2 (150 mL) and washed with H2O (3×50 mL). The organic portion was dried over Na2SO4 and evaporated to dryness in vacuo to provide N-[2-(2-bromomethyl-benzoyl)-4-chloro-phenyl]-benzamide (4.6 g, 74%). A solution of the benzamide (2.3 g, 5.4 mmol) in CH2Cl2 (50 mL) was saturated with dimethylamine, stirred for 16 h and evaporated to dryness in vacuo. The resulting residue was dissolved in MeOH (50 mL) and KOH (0.9 g, 16 mmol) in H2O (5 mL) was added. The solution was refluxed for 24 h. The solution was concentrated in vacuo and then diluted with EtOAc (150 mL) and H2O (50 mL). The organic portion was washed with H2O (3×50 mL), dried over Na2SO4 and purified by column chromatography (silica gel, 18:80:2 MeOH:CH2Cl2:NHOH) to provide 1q (0.9 g, 53% yield) MS m/z=289 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102678B2
Source datasetuspto-grants-2015_08
ORD IDord-4c754d4d62e74a058bca9b040d709ef1
Source noteuspto-grants-2015_08