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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413204Generated: October 26, 2026

Furfural → 2-(1-Hydroxy-2-methyl-3-butynyl)-furan

https://huagongshe.com/reaction/2413204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurfuralHCID 7362—
ReactantAmmonium ChlorideHCID 25517—
ReactantAluminumHCID 5359268—
Reactant3-Bromo-1-butyneHCID 10942465—
SolventTetrahydrofuranHCID 8028—
Product2-(1-Hydroxy-2-methyl-3-butynyl)-furanHCID 1336285058%

Reaction Steps

Aluminum (5.0 g, 0.18 mole), mercuric chloride (100 mg) and tetrahydrofuran (THF) (70 ml) were added to a reactor, and a solution of 3-bromo-1-butyne (20 g, 0.15 mole) in THF (20 ml) was added dropwise at 40° to 50° C. to prepare a Grignard reagent. Thereafter, to this THF solution of the Grignard reagent was added dropwise a solution of furfural (11.5 g, 0.12 mole) in THF (20 ml) at 20° to 30° C. over about 1 hour, followed by stirring at room temperature for further 2 hours. After completion of the reaction, the reaction solution was poured into an aqueous ammonium chloride solution (about 100 ml) and extracted with ether. The extract was washed with water, dried and concentrated. The residue obtained was distilled under reduced pressure to obtain 10.4 g (yield, 58%) of pure 1-(2-furyl)-2-methyl-3-butyn-1-ol having a boiling point of 75°-85° C./3 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04496586
Source datasetuspto-grants-1985_01
ORD IDord-b19be6b3b0944811b2c6cb4c85e6b0c3
Source noteuspto-grants-1985_01