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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868973Generated: October 30, 2026

Sodium hydride → (E)-3-(8-Methoxyquinolin-2-yl)acrylic acid

https://huagongshe.com/reaction/868973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantTrimethyl phosphonoacetateHCID 80029—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant8-Methoxyquinoline-2-carbaldehydeHCID 1548870—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(E)-3-(8-Methoxyquinolin-2-yl)acrylic acidHCID 7064878382.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of sodium hydride (60%) (0.8 mg, 20.0 mmol) in tetrahydrofuran (80 mL) was added methyl 2-(dimethoxyphosphoryl)acetate (2.65 mg, 12 mmol) dropwise at 0° C. After the addition was completed, the mixture was stirred for 30 min at 0° C. A solution of 8-methoxyquinoline-2-carbaldehyde (1.87 g, 10.0 mmol) in tetrahydrofuran (20 mL) was then added dropwise over a period of 50 min. The mixture was stirred at 0° C. for 1 h. A solution of lithium hydroxide hydrate (1.26 g, 30.0 mmol) in water (20 mL) was added cautiously to the solution. The resulting mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure. To the residue was added water (20 mL), and the pH of the aqueous layer was then adjust to 4 with 1 N hydrogen chloride solution. The precipitate was collected by filtration and then dried in vacuum to give 1.9 g of the product as a white solid. MS (ESI): m/z 230.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969349B2
Source datasetuspto-grants-2015_03
ORD IDord-b4c6c8424e4f43ccb7cde0aa72bb29e7
Source noteuspto-grants-2015_03