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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430890Generated: October 27, 2026

1-Bromo-2-chlorobenzene → N-(2-Chlorophenyl)-1,1-diphenylmethanimine

https://huagongshe.com/reaction/430890

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-chlorobenzeneHCID 12754—
ReactantBenzophenone imineHCID 136809—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductN-(2-Chlorophenyl)-1,1-diphenylmethanimineHCID 1564724671.3%

Reaction Steps

An oven-dried test tube was charged with tris(dibenzylideneacetone)dipalladium (4.6 mg, 0.005 mmol) and bis(2-(diphenylphosphino)phenyl)ether [DPE-phos] (8.2 mg, 0.015 mmol), capped with a rubber septum, evacuated, and refilled with argon. Benzophenone imine (190 mg, 1.05 mmol), 2-bromochlorobenzene (191 mg, 1.0 mmol) and toluene (2 mL) were added via syringe. The resulting solution was stirred at rt for 5 minutes. The tube was opened and sodium tert-butoxide (135 mg, 1.4 mmol) was added. The tube was again capped with the septum, and additional toluene (2 mL) was added via syringe to wash the solid from the test tube wall into the solution. The solution was stirred at room temperature with a gentle argon purge for 5 minutes, then heated at 80° C. for 2 hours and 5 minutes. The reaction mixture was cooled to room temperature and washed with saturated aqueous sodium chloride (2 mL). The organic layer was filtered through celite and concentrated in vacuo. The product was isolated as a yellow solid (208 mg, 71%) by flash chromatography on silica gel using 5% ethyl acetate in hexanes as eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323366B1
Source datasetuspto-grants-2001_11
ORD IDord-01e7abfc793f479c944d99e4091487ce
Source noteuspto-grants-2001_11