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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739559Generated: November 1, 2026

1,4-Dioxane → HCID 21841477, compound

https://huagongshe.com/reaction/1739559

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantBoronic AcidHCID 61668—
ReactantPotassium BromideHCID 253877—
ReactantHCID 21841495HCID 21841495—
CatalystHCID 178418397HCID 178418397—
ProductHCID 21841477HCID 21841477—

Reaction Steps

A mixture of 3 g of the product of Stage A, 1.66 g of boronic acid (Preparation 5), 3.5 g of monohydrated potassium phosphate, 1.32 g of potassium bromide and 300 mg of Pd(PPh3)4 (palladium tetrakis) in 50 ml of dioxane was refluxed for 12 hours. After pouring the reaction medium into a water-ice mixture, and carrying out extraction with ethyl acetate, the organic phase was dried, filtered and evaporated under reduced pressure. The crude product was purified by chromatography, eluting with a cyclohexane/ethyl acetate mixture (85/15) to obtain 1.95 g of the expected product with a Rf=0.05 (cyclohexane/ethyl acetate 85/15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965763
Source datasetuspto-grants-1999_10
ORD IDord-8af3af0223bd4f94b58f733c76d8edd0
Source noteuspto-grants-1999_10