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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170995Generated: November 4, 2026

Tetrabutylammonium Fluoride → 5-(4-Hydroxy-2,6-dimethylbenzyl)-2-methoxymethoxybenzaldehyde

https://huagongshe.com/reaction/1170995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant5-(2,6-Dimethyl-4-triisopropylsilanyloxybenzyl)-2-methoxymethoxybenzaldehydeHCID 86603457—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-(4-Hydroxy-2,6-dimethylbenzyl)-2-methoxymethoxybenzaldehydeHCID 8660345864%

Reaction Steps

To a solution of 5-(2,6-dimethyl-4-triisopropylsilanyloxybenzyl)-2-methoxymethoxy-benzaldehyde (1.4 g, 3.07 mmol) in THF (15 mL) was added TBAF (1 M, 3.68 mL) at 0° C. After stirring at r.t. for 2 h, the reaction mixture was diluted with EtOAc and water. The water layer was extracted with EtOAc and the combined organic extracts were dried (NgSO4), filtered and concentrated. The residue was purified by column chromatography on silica gel (ethyl acetate-hexanes; 1:9) to afford 5-(4-hydroxy-2,6-dimethylbenzyl)-2-methoxymethoxybenzaldehyde (590 mg, 64% for two steps): 1H NMR (200 MHz, CDCl3): δ 10.45 (s, 1H), 7.54 (s, 1H), 7.27 (m, 1H), 7.09 (m, 1H), 6.56 (s, 2H), 5.25 (s, 2H), 3.92 (s, 2H), 3.50 (s, 3H), 2.16 (s, 6H). TLC conditions: Uniplate silica gel, 250 microns; Mobile phase=ethyl acetate-hexanes (1:9); Rf=0.68.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829552B2
Source datasetuspto-grants-2010_11
ORD IDord-75de7dd4a5f243239800a4ebb917cb47
Source noteuspto-grants-2010_11