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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841838Generated: November 3, 2026

2-Bromopyridine → HCID 131732405, compound

https://huagongshe.com/reaction/1841838

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 131732406HCID 131732406—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131732405HCID 13173240525%

Reaction Steps

2-Bromopyridine (726 mg, 440 μl, 4.6 mmol) is dissolved in 5 ml of THF at ambient temperature. Isopropylmagnesium chloride (2.3 ml, 4.6 mmol, 2M in THF) is added dropwise under argon and the mixture is left stirring for 2 hours. This solution is added to a solution of tetraacetyl-(p-formylphenoxy)-β-galactose (2.07 g, 4.6 mmol) in 3 ml of THF at ambient temperature. The mixture is left stirring for 18 h and then a saturated NH4Cl solution is slowly added. The resulting aqueous solution is extracted with ethyl acetate. The organic phase is dried over Na2SO4 and evaporated under vacuum. The crude reaction product is purified by chromatography on silica gel (ether/pentane 2/1 pure ether). A yellow solid is then obtained (600 mg, yield 25%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08945514B2
Source datasetuspto-grants-2015_02
ORD IDord-7c21f2a8f03947a080178f64194575d1
Source noteuspto-grants-2015_02