HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481323Generated: October 27, 2026
Potassium tert-butoxide → 3,4-dihydro-2H-pyrano[2,3-b]pyridin-4-ol
https://huagongshe.com/reaction/1481323
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 1-(2-Chloropyridin-3-yl)propane-1,3-diol | HCID 59846570 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 3,4-dihydro-2H-pyrano[2,3-b]pyridin-4-ol | HCID 23049137 | — |
Reaction Steps
A mixture of 1-(2-chloropyridin-3-yl)propane-1,3-diol (62.9 mmol) and KOtBu (189 mmol) in 240 mL tBuOH (dried over 3 Å molsieves) was heated to 80° C. for 2.5 h. The reaction mixture was then concentrated to about ¼ of its volume, diluted with water and extracted 5 times with DCM. The combined organic layers were washed with brine, dried over MgSO4 and concentrated in vacuo. Purification with CC (KP-SIL™ from Biotage) using MeOH/DCM (99/1 to 95/5) gives the desired compound as orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409917B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-5bd51ae5cc2e4711b27dec943056cdfe |
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| Source note | uspto-grants-2016_08 |
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