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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085312Generated: November 1, 2026

Furfural → 1-(Furan-2-yl)but-3-en-1-ol

https://huagongshe.com/reaction/1085312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurfuralHCID 7362—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium BromideHCID 25514—
ReactantAmmonium ChlorideHCID 25517—
SolventTolueneHCID 1140—
Product1-(Furan-2-yl)but-3-en-1-olHCID 253052—

Reaction Steps

Reaction and after-treatment were carried out in the same manner as in Example 3 except that an equimolar amount of furfural was used in place of 5-methylfurfural, and that ammonium bromide and tetrahydrofuran were used in place of ammonium chloride and toluene, respectively, in the same weights as those of the latter, to obtain 50.6 g of the fraction of 2-(1-hydroxy-3-butenyl)-furan (content, 99.3%) (yield, 91.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05008410
Source datasetuspto-grants-1991_04
ORD IDord-f18e2fa4f5364ee6bc6a5b4e1034cc19
Source noteuspto-grants-1991_04