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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596477Generated: October 30, 2026

4-(2-Bromoethoxy)benzonitrile → HCID 69843550, compound

https://huagongshe.com/reaction/1596477

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Bromoethoxy)benzonitrileHCID 2452212—
ReactantTert-butyl 3,7-diazabicyclo(3.3.1)nonane-3-carboxylateHCID 22490264—
SolventAcetonitrileHCID 6342—
ProductHCID 69843550HCID 6984355072%

Reaction Conditions

Temperature60 °C

Reaction Steps

tert-Butyl-3,7-diazabicyclo[3.3.1]nonane-3-carboxylate (3.62 g; 16 mmol; see Example F above) was added to added to a stirred solution of 4-(2-bromoethoxy)benzonitrile (3.62g; 16 mmol; see Example 67(a) above) and TEA (3.34 mL; 24 mmol) in MeCN (70 mL) and the reaction mixture was stirred at 60° C. overnight and then stored at room temperature for 48 h. The solids were filtered off, washed with IPA (2×100 mL) and the filtrate concentrated. The residue was partitioned between DCM and NaHCO3 (sat.), the organic layer was separated, dried (MgSO4) and concentrated. The oily residue was subjected to column chromatography (DCM:MeOH; 25:1) to give the title compound in a 72% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291475B1
Source datasetuspto-grants-2001_09
ORD IDord-27b273b26bb44580ad913fd29a4765e5
Source noteuspto-grants-2001_09