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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046009Generated: October 25, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 3-Bromo-4-(2-chloro-5-fluorophenoxy)pyridine

https://huagongshe.com/reaction/1046009

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant3-Bromo-4-chloropyridineHCID 817696—
Reactant2-Chloro-5-fluorophenolHCID 2724522—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3-Bromo-4-(2-chloro-5-fluorophenoxy)pyridineHCID 6746669384%

Reaction Steps

A mixture of 2-chloro-5-fluorophenol (1.50 g, 10.24 mmol), 3-bromo-4-chloropyridine (1.50 g, 7.79 mmol) and DBU (1.50 g, 9.85 mmol) were heated at 130° C. in NMP (10 mL) for 15 hours. The reaction mixture was cooled and partitioned between water (100 mL) and MTBE (100 mL). The organic layer was separated, washed with dilute aq NaOH and brine, dried (MgSO4) and concentrated in vacuo to provide 3-bromo-4-(2-chloro-5-fluorophenoxy)pyridine (1.98 g, 84% yield) as brownish oil suitable for use in the next reaction. MS (ESI) m/z: 303.9 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569319B2
Source datasetuspto-grants-2013_10
ORD IDord-8ce7acec63df48f3ac58a9d011b3e58e
Source noteuspto-grants-2013_10