HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922453Generated: October 30, 2026
Water ethylacetate → HCID 86707865, compound
https://huagongshe.com/reaction/922453
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water ethylacetate | HCID 22728543 | — |
| Reactant | HCID 68784063 | HCID 68784063 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86707865 | HCID 86707865 | — |
Reaction Steps
To a solution of 6-bromo-1-(3-methoxypropyl)-1H-pyrrolo[3,2-b]pyridine (1.5 g) in toluene (30 mL) were added tri-n-butyltin-1-ethoxyvinyl (5.65 mL) and dichlorobis(triphenylphosphine)palladium (II) (782 mg), and the mixture was heated to stir at 110° C. for 30 minutes. The reaction solution was cooled to room temperature, and then thereto was added water-ethyl acetate, and an insoluble was filtered through Celite. The organic layer was separated, and then washed with saturated saline, dried over magnesium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by NH-silica gel column chromatography (eluent: n-hexane/ethyl acetate=4/1→1/1) to give 6-(1-ethoxyvinyl)-1-(3-methoxypropyl)-1H-pyrrolo[3,2-b]pyridine [REx(23-2)] (1.69 g) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278944B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-37ee25a27b1a4f4caecae929eeafbe28 |
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| Source note | uspto-grants-2016_03 |
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