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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Bis(pinacolato)diborane | HCID 2733548 | — |
| Reactant | 2-(5-bromoisochroman-1-yl)-4,5-dihydro-1H-imidazole | HCID 71766908 | — |
| Catalyst | HCID 178418851 | HCID 178418851 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4,5-Dihydro-1H-imidazol-2-yl)isochroman-5-ol | HCID 71767058 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249127B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-fceb03cb4e514b22ae649864b2cb8b0f |
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| Source note | uspto-grants-2016_02 |
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