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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204339Generated: October 31, 2026

Hydrochloric Acid → (5-Bromo-6-methoxy-pyridin-3-yl)-acetic acid

https://huagongshe.com/reaction/2204339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant5-Bromo-6-methoxy-3-pyridineacetonitrileHCID 58539392—
SolventEthanolHCID 702—
Product(5-Bromo-6-methoxy-pyridin-3-yl)-acetic acidHCID 82664957—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of (5-bromo-6-methoxy-pyridin-3-yl)-acetonitrile (Step AM1) (6.61 mmol) in EtOH (19 mL) was added a solution of KOH (26.7 mmol) in H2O (19 mL) and the mixture was stirred at 80° C. for 45 min. After cooling to rt, the pH was adjusted to 3-4 with 1M aqueous HCl and the mixture was extracted with CH2Cl2 (2×). The combined organic layers were dried (MgSO4), filtered and concentrated to afford the title compound. ESI-MS: tR=0.75 min, [M+H]+ 246/248 (LC-MS 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365576B2
Source datasetuspto-grants-2016_06
ORD IDord-853c5cd6c14c4984be132999887ea759
Source noteuspto-grants-2016_06