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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667616Generated: November 4, 2026

Iodine → HCID 58112003, compound

https://huagongshe.com/reaction/1667616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Bromopropionaldehyde dimethylacetalHCID 118932—
Reactant2-Bromo-N-methoxy-N-methylisonicotinamideHCID 44818654—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58112003HCID 5811200382.3%

Reaction Steps

To a suspension of Mg (3.67 g, 153.01 mmol) in THF (40 mL) is added cat. Iodine, followed by a solution of 3-bromo-1,1-dimethoxy-propane (21.47 g, 117.30 mmol) in THF (40 mL). The mixture is stirred at room temperature for 2 h. Then the fresh prepared Grignard reagent is cooled down in an ice bath, and added to a solution of 2-bromo-N-methoxy-N-methyl-isonicotinamide (12.50 g, 51.00 mmol) in THF (50 mL) at 0° C. The mixture is warmed up to room temperature and stirred at this temperature for 2 h. Then the reaction mixture is cooled in an ice bath, sat. NH4Cl and water are added and the mixture is extracted with EtOAc. The combined organic layers are washed with brine, dried over Na2SO4, filtered and concentrated down. The crude product is purified by flash chromatography on silica gel (EtOAc/Hexane: 10%) to give 1-(2-Bromo-pyridin-4-yl)-4,4-dimethyoxy-butane-1-one (12.1 g, 82%) as a pale yellow oil. M/Z=288.14

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044209B2
Source datasetuspto-grants-2011_10
ORD IDord-a0dc7b36f3dd44fe980c02652f290e29
Source noteuspto-grants-2011_10