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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654776Generated: October 25, 2026

Benzaldehyde → alpha-[(2-Furanyl)ethynyl]-benzenemethanol

https://huagongshe.com/reaction/1654776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantFuran, 2-ethynyl-HCID 140409—
ReactantLithium bis(trimethylsilyl)amideHCID 57426343—
SolventTetrahydrofuranHCID 8028—
Productalpha-[(2-Furanyl)ethynyl]-benzenemethanolHCID 20076917—

Reaction Steps

Place lithium hexamethyldisilazane (3 mL of a 1M solution in tetrahydrofuran, 3 mmol) under argon atmosphere and cool to 0° C. Add 2-furanylacetylene (276 mg, 3 mmol) in tetrahydrofuran (20 mL) and stir at 0° C. until anion formation is complete. Add a solution of benzaldehyde (297 mg, 2.8 mmol) in tetrahydrofuran, remove the ice bath and stir at room temperature until the reaction is complete. Pour onto ethyl ether and water, separate the organic layer and dry (MgSO4). Filter and evaporate the solvent in vacuo. Purify by silica gel chromatography to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05409942
Source datasetuspto-grants-1995_04
ORD IDord-2e9f376ed6604e7fa0f13a36388ca523
Source noteuspto-grants-1995_04