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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958392Generated: November 1, 2026

Hydrochloric Acid → 5-{[(Propan-2-yl)oxy]methyl}pyridine-2-carboxylic acid

https://huagongshe.com/reaction/1958392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant5-{[(Propan-2-yl)oxy]methyl}pyridine-2-carbonitrileHCID 21897415—
SolventEthanolHCID 702—
Product5-{[(Propan-2-yl)oxy]methyl}pyridine-2-carboxylic acidHCID 21897451—

Reaction Steps

In a 25 mL round-bottom flask was place ethanol (4 mL) solution of 5-isopropoxymethyl-pyridine-2-carbonitrile (1 g, 5.7 mmol). A solution of KOH (1.6 g, 28.36 mmol) in ethanol (6 mL) was added. The mixture was refluxed overnight and cooled down to room temperature. The resulted gel like mixture was added H2O and acidified with 6 mL of 10% HCl. The aqueous solution was extracted with EtOAc. The organic extracts were dried and concentrated to give the crude 5-isopropoxymethyl-pyridine-2-carboxylic acid. The crude product was further purified by column chromatography using 20% MeOH/CH2Cl2. 1H NMR (CDCl3, 400 MHz) δ 1.26 (d, 6H), 3.74 (m, 1H), 4.63 (s, 2H), 7.94 (d, 1H), 8.21 (m, 1H), 8.60 (s, 1H). Exact mass calculated for C10H13NO3 195.09, found 196.2 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410119B2
Source datasetuspto-grants-2013_04
ORD IDord-be10dc49c34c45f1a7227761b1e66ad7
Source noteuspto-grants-2013_04