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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
Reactant1-(2-Chloropyridin-3-yl)propane-1,3-diolHCID 59846570—
Solventtert-ButanolHCID 6386—
Product3,4-dihydro-2H-pyrano[2,3-b]pyridin-4-olHCID 23049137—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409917B2
Source datasetuspto-grants-2016_08
ORD IDord-5bd51ae5cc2e4711b27dec943056cdfe
Source noteuspto-grants-2016_08