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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228288Generated: November 1, 2026

Diethyl Ether → HCID 54398507, compound

https://huagongshe.com/reaction/2228288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium hydrideHCID 24758—
Reactant6-Bromopyridine-2-carbaldehydeHCID 2757009—
Reactant2-(Diethoxyphosphoryl)ethyl acetateHCID 12469628—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54398507HCID 5439850778.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

In THF (10 ml) was suspended sodium hydride (60%, 440 mg, 11.0 mmol), and to the mixture was added at −30° C. a solution of diethylphosphonoethyl acetate (2.47 g, 11.0 mmol) in THF (10 ml). The mixture was stirred at the same temperature for 30 minutes, and to the mixture was added at −30° C. a solution of 6-bromo-2-pyridinecarbaldehyde (1.86 g, 10.0 mmol) in THF (10 ml). While warming the temperature of the mixture from −30° C. to −10° C., the mixture was stirred for 1.5 hours. To the mixture was added diethylether (40 ml), and the mixture was washed with water (20 ml, 5 ml×2) and saturated brine (5 ml). The organic layer was dried with anhydrous magnesium sulfate and concentrated under reduced pressure. To the residue was added hexane (10 ml), and the mixture was cooled to 0° C. The precipitated insoluble materials were filtered, which were washed with hexane cooled to 0° C., and dried under reduced pressure to give ethyl 6-bromo-2-pyridineacrylate (2.00 g, 7.81 mmol, 78%). IR (KBr): 1717, 1703 cm−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413947B1
Source datasetuspto-grants-2002_07
ORD IDord-1851ddf7a195416ab8c3e42ed87c052c
Source noteuspto-grants-2002_07