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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656671Generated: November 2, 2026

Allyl Alcohol → 2-Allyloxy-tetrahydro-furan

https://huagongshe.com/reaction/1656671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
Reactant4-HydroxybutanalHCID 93093—
CatalystHydrochloric AcidHCID 313—
SolventHexaneHCID 8058—
Product2-Allyloxy-tetrahydro-furanHCID 52438193%

Reaction Steps

The procedure of Example 1 is followed with 4-hydroxybutanal (20.0 g of 11.5 wt. % solution, 26 mmol, 1.0 eq.), allyl alcohol (3.26 g, 56 mmol, 2.2 eq.), and hexanes (50 mL). Concentrated hydrochloric acid (2 drops) is used in place of the ion-exchange resin. After 3 h of stirring at room temperature, the hexane phase contains 8.8% of 2-allyloxytetrahydrofuran (3.1 g, 92.5% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05254702
Source datasetuspto-grants-1993_10
ORD IDord-6a3e1472f9c44701921563b0217e587b
Source noteuspto-grants-1993_10