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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771412Generated: November 4, 2026

1,4-Dioxane → 1-(4,5-Dihydro-1H-imidazol-2-yl)isochroman-5-ol

https://huagongshe.com/reaction/1771412

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantPotassium AcetateHCID 517044—
ReactantBis(pinacolato)diboraneHCID 2733548—
Reactant2-(5-bromoisochroman-1-yl)-4,5-dihydro-1H-imidazoleHCID 71766908—
CatalystHCID 178418851HCID 178418851—
SolventDimethylformamideHCID 6228—
Product1-(4,5-Dihydro-1H-imidazol-2-yl)isochroman-5-olHCID 71767058—

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 2-(5-bromoisochroman-1-yl)-4,5-dihydro-1H-imidazole (720 mg), bis(pinacolato)diboron (715 mg) bis(tri-t-butylphosphine)palladium(0) (39 mg), potassiumacetate (503 mg), dioxane (9 ml) and DMF (0.75 ml) was stirred under inert atmosphere in microwave reactor at 160° C. for 30 minutes. Additional bis(tri-t-butylphosphine)palladium(0) (21 mg) was added and heating continued for 15 minutes. The intermediate 2-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isochroman-1-yl)-4,5-dihydro-1H-imidazole (680 mg) was purified with separation method A and stirred with EtOAc (2 ml), water (2 mil) and hydrogen peroxide (35%, 0.07 ml) at ice bath temperature for 2 hrs. The title compound was purified with separation methods A and E. (Yield 45 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249127B2
Source datasetuspto-grants-2016_02
ORD IDord-fceb03cb4e514b22ae649864b2cb8b0f
Source noteuspto-grants-2016_02