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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413202Generated: November 1, 2026

Furfural → HCID 11788394, compound

https://huagongshe.com/reaction/2413202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurfuralHCID 7362—
Reactant3-Chloro-1-buteneHCID 11242—
ReactantCrotyl chlorideHCID 11589—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11788394HCID 1178839490%

Reaction Steps

Magnesium (36 g, 1.5 mole) and tetrahydrofuran (THF) (300 ml) were added to a reactor, and a solution of crotyl chloride or 3-chloro-1-butene (118 g, 1.8 mole) in THF (100 ml) was added dropwise at 30° to 35° C. to prepare a Grignard reagent. Thereafter, to this THF solution of the Grignard reagent was added dropwise a solution of furfural (106 g, 1.1 mole) in THF (150 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 500 ml), followed by extraction with ether. The ether extract was washed with water, dried and concentrated, and the residue obtained was distilled under reduced pressure to obtain 150 g (yield, 90%) of pure 1-(2-furyl)-2-methyl-3-buten-1-ol having a boiling point of 95°-107° C./25 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04496586
Source datasetuspto-grants-1985_01
ORD IDord-50d0eea3e396417f83f0293318d469d2
Source noteuspto-grants-1985_01