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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49804Generated: October 26, 2026

Bromine → HCID 178524767, compound

https://huagongshe.com/reaction/49804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantHCID 178418479HCID 178418479—
SolventWaterHCID 962—
ProductHCID 178524767HCID 17852476797%

Reaction Steps

Bromine (4.2 mL, 81.4 mmol) was added dropwise to the suspension of 6-hydroxynicotinic acid Compound 116a (8.00 g, 57.6 mmol) in water (30 mL) at 4° C. After the completion of the addition, the cooling bath was removed and the reaction mixture was stirred at room temperature for 4 h. Saturated Na2SO5 was added slowly to the stirred mixture until the brown mixture became white. The solid was collected through filtration, washed with water, and dried under vacuum overnight to give 12.17 g (97%) of 6-hydroxy-5-bromonicotinic acid as an off-white solid; 1H NMR (300 MHz, DMSO-d6) δ12.95 (brs, 1H), 12.55 (brs, 1H), 8.16 (s, 1H), 8.04 (s, 1H). Quinoline (1.0 mL, 8.47 mmol) was slowly added to the solution of POCl3 (2.0 mL, 21.5 mmol), followed by 6-hydroxy-5-bromonicotinic acid (3.92 g, 18.0 mmol) at room temperature. After heating at 120° C. for 2 h, the reaction was quenched by addition of water dropwise at 10° C. After the mixture was cooled at 4° C. for a few hours, the solid was collected through filtration, washed with water, and dried under vacuum overnight to give 3.68 g (87%) of Compound 116b as an off-white solid; 1H NMR (300 MHz, DMSO-d6) δ8.86 (s, 1H), 8.55 (s, 1H); MS (ES) m/z: 236 (M−H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710048B2
Source datasetuspto-grants-2004_03
ORD IDord-c0d8ea08cb614f1eab6303a8ae1e26f4
Source noteuspto-grants-2004_03