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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793306Generated: November 1, 2026

Ammonium Chloride → (2H-[1,3]Dioxolo[4,5-b]pyridin-2-yl)methanol

https://huagongshe.com/reaction/1793306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 22020963HCID 22020963—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(2H-[1,3]Dioxolo[4,5-b]pyridin-2-yl)methanolHCID 2202093743.2%

Reaction Steps

Reaction under a nitrogen atmosphere. A solution of intermediate (4) (0.042 mol) in THF (48 ml) was added dropwise to LiAlH4 (1 Min THF) (0.0466 mol) and cooled with an ice-water bath. The resulting reaction mixture was stirred for one hour at room temperature. The reaction mixture was treated carefully with a 10% NH4Cl solution and it was diluted with water and ethyl acetate. The reaction mixture was filtered over Celite and the filtrate was extracted. The separated organic layer was dried, filtered and the solvent was evaporated. The residue was washed with DCM, filtered off and dried, yielding 2.78 g of (±)-1,3-dioxolo[4,5-b]pyridine-2-methanol (intermediate 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07081453B2
Source datasetuspto-grants-2006_07
ORD IDord-52bd9af9abde4dd88619b3dcdc6bb275
Source noteuspto-grants-2006_07