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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430886Generated: October 31, 2026

3-Bromoanisole → HCID 15545157, compound

https://huagongshe.com/reaction/430886

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromoanisoleHCID 16971—
ReactantBenzophenone imineHCID 136809—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
SolventTolueneHCID 1140—
ProductHCID 15545157HCID 1554515783%

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), 3-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 5 minutes, then heated at 80° C. for 5 hours and 40 minutes. The reaction mixture was cooled to room temperature, washed with saturated aqueous sodium chloride (2 mL), and the organic layer was concentrated in vacuo. The product was isolated as a yellow oil (237 mg, 83%) 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-c790eac53cb8447cb1aec50742e5a990
Source noteuspto-grants-2001_11