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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600926Generated: November 3, 2026

Toluene → HCID 21830644, compound

https://huagongshe.com/reaction/1600926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant3-Fluorophenylboronic acidHCID 2733986—
ReactantHCID 21717163HCID 21717163—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
ProductHCID 21830644HCID 2183064460.7%

Reaction Conditions

Temperature120 °C

Reaction Steps

Prepared according to the method described in Example 33a) from toluene (5 ml), aqueous sodium carbonate (2 M, 2.2 ml), (±)-3-(4(4-bromophenoxy)-3-(tert-butyldimethylsilyloxy)butyl)pyridine (0.79 g), ethanol (1.3 ml), 3-fluorobenzeneboronic acid (0.25 g) and tetrakis(triphenylphosphine)palladium(0) (72 mg) with heating at 120° C. for 6 hours. The residue obtained after work up was purified by column chromatography over silica to give the sub-title compound as an oil (0.49 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977105
Source datasetuspto-grants-1999_11
ORD IDord-3cdeb3214e0b427cb18db4e270ac5b1c
Source noteuspto-grants-1999_11