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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696702Generated: October 31, 2026

Propanal → HCID 67276554, compound

https://huagongshe.com/reaction/1696702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropanalHCID 527—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Benzyloxy-5-bromopyridineHCID 11108191—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67276554HCID 6727655464%

Reaction Conditions

Temperature-78 °C

Reaction Steps

In a nitrogen atmosphere at −78° C., 2.71 M n-BuLi/hexane solution (18.8 mL) was dropwise added to a THF solution of 2-(benzyloxy)-5-bromopyridine (12.2 g, 46.2 mmol) synthesized according to the method described in a reference (J. Org. Chem., 1995, Vol. 60, p. 1408), and stirred at −78° C. for 1 hour. At −78° C., propionaldehyde (4.3 mL) was dropwise added, and stirred at −78° C. for 30 minutes and then at room temperature for 3 hours. Aqueous saturated ammonium chloride solution was added to the reaction liquid, and extracted with ethyl acetate. The organic layer was washed with saturated saline, then dried with magnesium sulfate and concentrated. This was purified by silica gel column chromatography to obtain the intended compound (7.15 g, 64%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163770B2
Source datasetuspto-grants-2012_04
ORD IDord-41473cbaaf3d4bf682df948ff6fbb9ad
Source noteuspto-grants-2012_04