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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192361Generated: November 4, 2026

1-((2-Bromoethoxy)methyl)-4-methoxybenzene → HCID 67311654, compound

https://huagongshe.com/reaction/2192361

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-((2-Bromoethoxy)methyl)-4-methoxybenzeneHCID 11701510—
Reactant1-Phenyl-cycloheptanecarboxylic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl)esterHCID 59179619—
SolventAcetonitrileHCID 6342—
ProductHCID 67311654HCID 67311654148.6%

Reaction Steps

A mixture of 1-(2-bromo-ethoxymethyl)-4-methoxy-benzene (42 mg) and 1-phenyl-cycloheptanecarboxylic acid (R)-(1-aza-bicyclo[2.2.2]oct-3-yl)ester (Example 14e) (50 mg) in MeCN (1 mL) was stirred at room temperature for 16 h then heated to 80° C. under nitrogen overnight. A further 1.1 equivalents of 1-(2-bromo-ethoxymethyl)-4-methoxy -benzene were added and the mixture was heated at 80° C. for a further 48 h. The volatiles were evaporated and the crude product was purified by silica gel chromatography eluting with 0-10% of a 10% conc. NH3/MeOH solution in dichloromethane give 61 mg of an oil that was purified further by reverse phase HPLC (Gemini 5 μM C6 phenyl column) eluting with 5-95% MeOH/H2O containing 0.1% formic acid over 30 min with UV detection at 220 nm. The relevant fractions were combined and evaporated to afford the title compound (34 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329729B2
Source datasetuspto-grants-2012_12
ORD IDord-00ca82777f5e4b7890fe7f4147cac5ab
Source noteuspto-grants-2012_12