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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484826Generated: October 31, 2026

1,4-Dioxane → HCID 22628954, compound

https://huagongshe.com/reaction/1484826

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant4-Chlorophenylboronic acidHCID 74299—
ReactantSodium BicarbonateHCID 516892—
Reactant(2-Chloropyridin-3-yl)methanolHCID 2763647—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
ProductHCID 22628954HCID 2262895465.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

Into a 100-mL round-bottom flask, was placed a solution of (4-chlorophenyl)boronic acid (1.6 g, 10.23 mmol, 1.20 equiv), (2-chloropyridin-3-yl)methanol (1 g, 6.97 mmol, 1.00 equiv), Pd(dppf)Cl2 (570 mg, 0.78 mmol, 0.10 equiv), and sodium bicarbonate (1.7 g, 20.24 mmol, 3.00 equiv) in a solvent mixture of dioxane (10 mL) and water (10 mL). The resulting solution was stirred for 4 h at 70° C., and then it was diluted with 100 mL of H2O. The resulting solution was extracted with 2×200 mL of dichloromethane, and the combined organic layers were concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:100-1:5) as eluent to yield 1 g (65%) of [2-(4-chlorophenyl)pyridin-3-yl]methanol as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422279B2
Source datasetuspto-grants-2016_08
ORD IDord-bd5fab8e52ec406cafd632f0f726984f
Source noteuspto-grants-2016_08