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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15492Generated: November 1, 2026

Tetrabutylammonium Fluoride → (R)-2-(9-(1H-1,2,3-Triazol-1-yl)nonyl)-2,5,7,8-tetramethylchroman-6-ol

https://huagongshe.com/reaction/15492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant(R)-1-(9-(6-(tert-butyldimethylsilyloxy)-2,5,7,8-tetramethylchroman-2-yl)nonyl)-1H-1,2,3-triazoleHCID 25118684—
SolventTetrahydrofuranHCID 8028—
Product(R)-2-(9-(1H-1,2,3-Triazol-1-yl)nonyl)-2,5,7,8-tetramethylchroman-6-olHCID 25119043—

Reaction Steps

A solution of tetrabutylammonium fluoride (TBAF) (1M in THF, 250 μL) was added dropwise via syringe to a stirred solution of (R)-1-(9-(6-(tert-butyldimethylsilyloxy)-2,5,7,8-tetramethylchroman-2-yl)nonyl)-1H-1,2,3-triazole (65 mg, 0.126 mmol) in dry THF (5 ml). The mixture was stirred at room temperature for 30 minutes until starting material was not detected by TLC. The reaction was then quenched with 500 μL of 1N HCl and diluted with 25 ml of ether, to which an additional 10 ml of dH2O was added. The water phase was extracted again with ether (2×25 ml), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The crude product was chromatographed on silica gel (Et2O) to give the pure product (TLC Rf=0.49, EtOAc) as an off-white/yellow solid. (35 mg, 70%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732617B2
Source datasetuspto-grants-2010_06
ORD IDord-ecb997b2c8a34a65b93c81a56497c052
Source noteuspto-grants-2010_06