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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594304Generated: November 2, 2026

Diisobutylaluminum hydride → [6-(Difluoromethoxy)pyridin-2-yl]methanol

https://huagongshe.com/reaction/594304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantSodium HydroxideHCID 14798—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 6-(difluoromethoxy)picolinateHCID 69081734—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product[6-(Difluoromethoxy)pyridin-2-yl]methanolHCID 69083466—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A cooled (−78° C.) solution of methyl 6-(difluoromethoxy)picolinate (4.310 g; 21.21 mmol) in anh. toluene (120 ml) was treated dropwise with a solution of 1 M DIBAH in toluene (63.60 ml; 63.60 mmol), and the resulting mixture was further stirred at −78° C., under nitrogen, for 5 min., and then at 0° C. for 1.5 h. The obtained mixture was treated successively with water (55 ml), 1 M aq. NaOH (12 ml), and aq. sat. NaHCO3 (100 ml). The separated aq. layer was further extracted with Et2O (2×100 ml). The mixed organic layers were then dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure affording (6-(difluoromethoxy)pyridin-2-yl)methanol as a yellow oil (3.310 g; 89%). LC-MS (conditions D): tR=0.76 min.; no ionisation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-955bd79727894b6892ed1db1060b6d5e
Source noteuspto-grants-2016_01