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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443648Generated: October 26, 2026

Tetrabutylammonium Fluoride → 7-[4-(4-Methoxyphenyl)thiazol-2-yl]heptan-1-ol

https://huagongshe.com/reaction/1443648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant2-[7-(Tert-butyldimethylsilanyloxy)heptyl]-4-(4-methoxyphenyl)thiazoleHCID 68489930—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product7-[4-(4-Methoxyphenyl)thiazol-2-yl]heptan-1-olHCID 6849141189.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Add a solution of 1 N tetra-n-butylammonium fluoride (25.0 mmol, 25 mL, 1 M solution in THF) dropwise over 10 minutes to a solution of 2-[7-(tert-butyldimethylsilanyloxy)heptyl]-4-(4-methoxyphenyl)thiazole (6.27 g, 14.9 mmol) in anhydrous THF (50 mL) at 0° C. under nitrogen and stir the mixture for 30 minutes at 0° C. and then stir at room temperature for 3 hours. Dilute the mixture with brine (150 mL) and extract with ethyl acetate (100 mL×3). Dry the combined organic extracts over magnesium sulfate and remove the solvent under reduced pressure. Purify the crude product by flash column chromatography on silica gel, eluting with ethyl acetate/hexanes (1:2), to give 7-[4-(4-methoxyphenyl)thiazol-2-yl]heptan-1-ol (4.07 g, 89%): APCI mass spectrum m/z 306 [C17H23NO2S+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662771B2
Source datasetuspto-grants-2010_02
ORD IDord-15ee9b6c030246e9a91163570dfab67f
Source noteuspto-grants-2010_02