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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266377Generated: November 2, 2026

Hydrochloric Acid → 2-Fluoro-4-iodopyridine-3-carboxylic acid

https://huagongshe.com/reaction/2266377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Methyl-2-buteneHCID 10553—
ReactantTrisodium PhosphateHCID 24243—
Reactant2-Fluoro-4-iodopyridine-3-carbaldehydeHCID 9992328—
ReactantSodium ChloriteHCID 23668197—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Solventtert-ButanolHCID 6386—
Product2-Fluoro-4-iodopyridine-3-carboxylic acidHCID 44754754100%

Reaction Steps

To a stirred solution of 2-fluoro-4-iodopyridine-3-carboxaldehyde (10.0 g, 39.8 mmol) in tert-butanol (350 mL) and water (100 mL) at room temperature were added 2-methyl-2-butene (42.1 ml, 398 mmol), sodium phosphate, monobasic, monohydrate (60.5 g, 438 mmol) and sodium chlorite (18.0 g, 199 mmol). The reaction mixture was stirred at room temperature for 75 min. The reaction mixture was diluted with dichloromethane and a 6M aqueous solution of hydrochloric acid was added until pH ˜2. The water layer was extracted with dichloromethane. The organic phase was dried over MgSO4, filtered and concentrated in vacuo. Purification by MPLC (CH2Cl2/MeOH+1% AcOH: 100/0 to 80/20) afforded 2-fluoro-4-iodonicotinic acid (10.63 g, 39.8 mmol, 100% yield). MS (ESI pos. ion) m/z: 268 (MH+). Calc'd exact mass for C6H3FINO2: 267.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858623B2
Source datasetuspto-grants-2010_12
ORD IDord-ec4761a6e46e41fcaa675aa441f4682a
Source noteuspto-grants-2010_12