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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085313Generated: October 30, 2026

Furfural → 1-(2-Furyl)but-3-yn-1-ol

https://huagongshe.com/reaction/1085313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurfuralHCID 7362—
ReactantTetrahydrofuranHCID 8028—
CatalystHexadecyltrimethylammonium chlorideHCID 8154—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
Product1-(2-Furyl)but-3-yn-1-olHCID 10909623—

Reaction Steps

Reaction and after-treatment were carried out in the same manner as in Example 16 except that an equimolar amount of furfural was used in place of 5-methylfurfural, and that cetyltrimethylammonium chloride and tetrahydrofuran were used in place of tetrabutylammonium bromide and toluene, respectively, in the same weights as those of the latter, to obtain 44.0 g of the fraction of 2-(1-hydroxy-3-butynyl)furan (content, 99.4%) (yield, 80.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05008410
Source datasetuspto-grants-1991_04
ORD IDord-959441cff14e4650a87cbfc07e6b7d88
Source noteuspto-grants-1991_04