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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786566Generated: October 30, 2026

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

https://huagongshe.com/reaction/1786566

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 numberUS07507754B2
Source datasetuspto-grants-2009_03
ORD IDord-ac2ef776a5ec4e41aedf2abf920d3586
Source noteuspto-grants-2009_03