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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75473Generated: October 26, 2026

Dimethylformamide → 2-(Pyridin-3-yloxy)ethan-1-ol

https://huagongshe.com/reaction/75473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantEthylene carbonateHCID 7303—
Reactant3-HydroxypyridineHCID 7971—
ReactantPotassium CarbonateHCID 11430—
CatalystEthylene carbonateHCID 7303—
SolventWaterHCID 962—
Product2-(Pyridin-3-yloxy)ethan-1-olHCID 2190899772%

Reaction Conditions

Temperature86 °C

Reaction Steps

3-hydroxypyridine (20.0 kg), ethylene carbonate (19.4 kg), K2CO3 (18.9 kg), and DMF (75.5 kg) were charged to a 400 L reactor and heated to 86° C. After 13H, an aliquot was taken. There was still some 3-hydroxypyridine left by GC so more ethylene carbonate (1.0 kg) was added. After 20H, the reaction was deemed complete. The reaction was cooled to 20° C., H2O (85 L) was slowly added to the 400 L reactor, and stirring continued for 30 min. The title compound was extracted with 35° C. CH2Cl2 (4×170 L) sending the CH2Cl2 extractions into the 1000 L portable tank. The aqueous layer was discarded, and the 400 L reactor was cleaned. The solution of the title compound in the 1000 L portable tank was transferred to the 400 L and distilled in the 400 L reactor sending the distillate to the 400 L receiver. Toluene (200 L) was added so the 400 L reactor and distilled sending the distillate to the 400 L receiver. The resulting oil was transferred to a 20 L glass bottle to produce 21.0 kg (72%) of the title compound of 100.0% GC purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835439B2
Source datasetuspto-grants-2014_09
ORD IDord-ffd687ac69c54711aaca5846f746f590
Source noteuspto-grants-2014_09