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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490336Generated: October 29, 2026

Tetrabutylammonium Fluoride → Methyl 4-(hydroxymethyl)-5-methylfuran-2-carboxylate

https://huagongshe.com/reaction/490336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant5-Methyl-4-triisopropylsilanyloxymethyl-furan-2-carboxylic acid methyl esterHCID 58824202—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(hydroxymethyl)-5-methylfuran-2-carboxylateHCID 58824163—

Reaction Steps

A stirred solution of 5-methyl-4-triisopropylsilanyloxymethyl-furan-2-carboxylic acid methyl ester (15) (5.2 g) in tetrahydrofuran (200 mL) was treated with tetrabutylammonium fluoride (1.0 M solution in tetrahydrofuran, 3.2 mL) and stirring continued for 16 hours. The reaction mixture was concentrated in vacuo and the residue taken up in ethyl acetate (350 mL) and washed with water (150 mL). The aqueous phase was re-extracted with ethyl acetate (2×100 mL). The combined extracts were dried, concentrated in vacuo and the residue was purified by flash chromatography eluting with ethyl acetate/pentane (1:1 by volume) to give compound 16 as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528157B2
Source datasetuspto-grants-2009_05
ORD IDord-f275f8a838d74f7e9e534b8303c94fac
Source noteuspto-grants-2009_05