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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475636Generated: October 30, 2026

1-Bromo-4-fluorobenzene → HCID 68170292, compound

https://huagongshe.com/reaction/1475636

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
Reactanttert-Butyl cyclopentylacetateHCID 10797592—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductHCID 68170292HCID 68170292—

Reaction Steps

Under argon, a solution of 2.0 g (10.85 mmol) of tert-butyl cyclopentylacetate in 5 ml of abs. toluene was added dropwise to 16.3 ml of a 1 M solution, cooled to −10° C., of lithium hexamethyl-disilazide in toluene (16.3 mmol). After 10 min at −10° C., the ice bath was removed and the mixture was warmed to RT. A mixture of 2.47 g (14.1 mmol) of 1-bromo-4-fluorobenzene, 73.1 mg (0.326 mmol) of palladium(II) acetate and 269 mg (0.684 mmol) of 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl in 10 ml of abs. toluene was then added to this reaction mixture. After 1 h at RT, the reaction mixture was stirred at 80° C. overnight. After cooling to RT, the precipitated salts were filtered off with suction, the residue was washed with toluene and the combined filtrates were concentrated under reduced pressure. The crude product obtained was purified chromatographically on silica gel (mobile phase first cyclohexane, then cyclohexane/ethyl acetate 50:1). This gave 2.0 g of the title compound (61.6% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018258B2
Source datasetuspto-grants-2015_04
ORD IDord-eb257e6954d24ad5a7a4d4ddfc453a88
Source noteuspto-grants-2015_04