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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430888Generated: October 31, 2026

2-Bromoanisole → HCID 1236184, compound

https://huagongshe.com/reaction/430888

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoanisoleHCID 11358—
ReactantBenzophenone imineHCID 136809—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 1236184HCID 123618475.2%

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-bromoanisole (187 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 23 minutes, then heated at 80° C. for 2 hours and 10 minutes. The reaction mixture was cooled to room temperature and 1 mL ether was added. This solution was washed with saturated aqueous sodium chloride (2 mL) and the organic layer was concentrated in vacuo. The product was isolated as a yellow oil (216 mg, 75%) by flash chromatography on silica gel using 10% ethyl acetate in hexanes as eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323366B1
Source datasetuspto-grants-2001_11
ORD IDord-20d72354aa12443c86d098ba6608033d
Source noteuspto-grants-2001_11