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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383003Generated: October 31, 2026

Sodium Hydroxide → (Furo[3,2-c]pyridin-6-yl)methanol

https://huagongshe.com/reaction/1383003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 21273331HCID 21273331—
SolventHydrochloric AcidHCID 313—
SolventAcetic AnhydrideHCID 7918—
Product(Furo[3,2-c]pyridin-6-yl)methanolHCID 1400523464%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 6-methylfuro[3,2-c]pyridine-N-oxide monohydrate (19.85 g, 0.119 mol) in acetic anhydride (30 mL) was heated at 100° C. for one half hour. Then the reaction mixture was diluted with 20% hydrochloric acid (100 mL) and heating was continued for one hour. The solution was cooled and made basic with sodium hydroxide solution. The product was extracted into chloroform, dried over anhydrous sodium sulfate, filtered through a pad of charcoal and evaporated. The residue was triturated with cool benzene and the crystalline product collected by filtration to give 11.36 g (64% yield), mp: 72°-74° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04808595
Source datasetuspto-grants-1989_02
ORD IDord-a409d72270784fcf98f40e0d728af78f
Source noteuspto-grants-1989_02