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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025388Generated: November 1, 2026

Iodine → HCID 46913420, compound

https://huagongshe.com/reaction/1025388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantMethanolHCID 887—
ReactantSodium AcetateHCID 517045—
Reactant6-Bromoimidazo[1,2-a]pyridineHCID 2795547—
Reactant6-Bromo-3-iodoimidazo(1,2-a)pyridineHCID 22031632—
ProductHCID 46913420HCID 46913420—

Reaction Conditions

Temperature0 °C

Reaction Steps

6-bromo-3-iodoimidazo[1,2-a]pyridine. To a 150 mL round bottomed flask was added 6-bromoimidazo[1,2-a]pyridine (5.00 g, 25.4 mmol), anhydrous sodium acetate (5.69 g, 69.4 mmol) and MeOH (60 mL). The resulting mixture was cooled to 0° C. followed by adding iodine (7.13 g, 28.1 mmol). After the addition, ice bath was removed. It was warmed up to rt and continued to stir for 20 h. The precipitate in the reaction mixture was collected by filtration. The precipitate was washed with MeOH and dried to afford the desired product as light grey solid (7.0 g). MS (ESI pos. ion) m/z: 322.8. Calcd exact mass for C7H4BrIN2: 321.9. 1H NMR (300 MHz, CHLOROFORM-d) δ ppm 7.30 (d, J=10.82 Hz, 1H) 7.52 (d, J=9.50 Hz, 1H) 7.71 (s, 1H) 8.29 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729074B2
Source datasetuspto-grants-2014_05
ORD IDord-1a0b96fbb4f44861aabd4a062fe7d89b
Source noteuspto-grants-2014_05