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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192349Generated: October 29, 2026

5-(2-Bromoethyl)-2,3-dihydro-1-benzofuran → HCID 44516993, compound

https://huagongshe.com/reaction/2192349

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(2-Bromoethyl)-2,3-dihydro-1-benzofuranHCID 21831160—
Reactant1-Phenyl-cycloheptanecarboxylic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl)esterHCID 59179619—
SolventAcetonitrileHCID 6342—
ProductHCID 44516993HCID 4451699370%

Reaction Steps

A mixture of 1-phenyl-cycloheptanecarboxylic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl) ester (Example 14e) (126 mg) and 5-(2-bromo-ethyl)-2,3-dihydro-benzofuran (105 mg, 0.46 mmol) in acetonitrile (1.5 mL) was stirred at room temperature for 22 h. The volatiles were evaporated and the residue purified by silica gel chromatography eluting with dichloromethane then 5% then 10% MeOH/dichloromethane. The relevant fractions were combined and evaporated and the residue triturated with dichloromethane to give an off -white foam. Further purification was achieved by reverse-phase HPLC (5-98% MeCN containing 0.1% formic acid) to give the title compound (70 mg) as a white gummy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329729B2
Source datasetuspto-grants-2012_12
ORD IDord-a0d50768ca8f48daa3a97b30c2b1bd21
Source noteuspto-grants-2012_12