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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 993284Generated: October 29, 2026

Hydrochloric Acid → HCID 22145686, compound

https://huagongshe.com/reaction/993284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium TetrafluoroborateHCID 4343483—
ReactantMethyl 5-amino-6-methoxypyridine-3-carboxylateHCID 22145836—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
ProductHCID 22145686HCID 2214568686.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Concentrated hydrochloric acid (9.06 mL of strength 36%) is added to a stirred suspension of methyl 5-amino-6-methoxynicotinoate (3.3 g) in water (20 mL). The mixture is cooled to 0° C. and treated dropwise with a solution of sodium nitrite (1.37 g) in water (5 mL). After 30 minutes at 0° C. a solution of sodium tetrafluoroborate (2.84 g) in water (10 mL) is added. After a further 30 minutes the precipitated diazonium salt is collected, washed with a little ice-cold water then with diethyl ether and sucked dry. Potassium carbonate (1.0 g) is added to trifluoroacetic acid (32 mL) at 0° C. followed by the addition of the diazonium salt in one portion. The mixture is stirred at reflux for 18 hours, cooled then poured into iced water and stirred for 1 hour. The aqueous mixture is neutralised with solid sodium bicarbonate and extracted with ethyl acetate. The extracts are washed with water and dried (MgSO4). Concentration afforded methyl 5-hydroxy-6-methoxynicotinoate (2.86 g) as a beige solid. This material is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06472412B1
Source datasetuspto-grants-2002_10
ORD IDord-598d87a167d84f479a74e749c24babe8
Source noteuspto-grants-2002_10