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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357282Generated: October 30, 2026

Hydrochloric Acid → 2-[(2,6-Dichloro-3-methylphenyl)amino]benzaldehyde

https://huagongshe.com/reaction/357282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant2-[(2,6-Dichloro-4-methylphenyl)amino]benzoic acidHCID 18936982—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product2-[(2,6-Dichloro-3-methylphenyl)amino]benzaldehydeHCID 15027377120.7%

Reaction Steps

A mixture in dry dichloromethane (135 mL) of 2-[(2,6-dichloro-4-methylphenyl)amino]benzoic acid (meclofenamic acid) (7.0 g, 23.6 mmol), N,O-dimethylhydroxylamine hydrochloride (5.0 g, 51.9 mmol), carbon tetrabromide (17.2 g, 51.9 mmol), triphenylphosphine (13.6 g, 51.9 mmol), and pyridine (10 mL) was stirred at ambient temperature for 48 hours. The reaction mixture was poured into 10% HCl (100 mL) and extracted with ethyl acetate (3×200 mL). The combined organic layers were washed with water and brine, dried over MgSO4, filtered, and evaporated in vacuo. Purification by chromatography on silica gel (9:1 hexane/ethyl acetate) provided 7.98 g (99%) of 2-[(2,6-dichloro-3-methylphenyl)amino]benzaldehyde as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840758
Source datasetuspto-grants-1998_11
ORD IDord-eea4ac23e351495a8deb42c525e825c6
Source noteuspto-grants-1998_11