Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038657Generated: October 31, 2026

Iodine → HCID 58191784, compound

https://huagongshe.com/reaction/1038657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Bromopropionaldehyde dimethylacetalHCID 118932—
Reactant2-Chloro-5-fluoropyridine-4-carbaldehydeHCID 44754755—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58191784HCID 5819178425%

Reaction Steps

To a solution of Mg (0.71 g, 30 mmol) in THF (10 mL) are added cat iodine and a solution of 3-bromo-1,1-dimethoxy-propane (3.99 g, 21.57 mmol) in THF (10 mL). The mixture is stirred at room temperature for 2 hours. At −30° C., to a solution of 2-chloro-5-fluoro-pyridine-4-carbaldehyde (2.0 g, 12.54 mmol) in THF (5 mL) is added to the above prepared Grignard reagent. The mixture is stirred at this temperature for 2 hours. Then the reaction mixture is cooled in an ice bath, saturated 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 chromatography (EtOAc/hexane: 10%˜40%) to give 1-(2-chloro-5-fluoro-pyridin-4-yl)-4,4-dimethoxy-butan-1-ol (0.81 g, 25%). M/Z=264.13[M+1]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552003B2
Source datasetuspto-grants-2013_10
ORD IDord-74e4ed81c3a04b738ab1d274afbb7544
Source noteuspto-grants-2013_10