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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 886690Generated: November 1, 2026

(Trifluoromethyl)trimethylsilane → 1,1,1-Trifluoro-3-[(benzyl)oxy]-2-{[(benzyl)oxy]methyl}-2-propanol

https://huagongshe.com/reaction/886690

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant1,3-Bis(benzyloxy)propan-2-oneHCID 11391582—
ReactantTetrabutylammonium Fluoride TrihydrateHCID 11726816—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product1,1,1-Trifluoro-3-[(benzyl)oxy]-2-{[(benzyl)oxy]methyl}-2-propanolHCID 24809783101.8%

Reaction Steps

Tetrabutylammonium fluoride trihydrate (TBAF 3H2O) (2.9 g, 0.5 equivalent) was dissolved in THF (5 ml). This was added cautiously to a stirred and cooled (+15° C.) solution of 1,3-dibenzyloxy-2-propanone in toluene (24.65 g, equivalent to 5 g of the ketone) and (trifluoromethyl)trimethylsilane (7.5 ml). There was an exotherm and a lot of gas evolution on addition of the first 1 ml of TBAF solution. The temperature rose from 18 to 40° C. The TBAF addition was carried out over 3 minutes and then the mixture was stirred at 15-30° C. for a further 2 minutes and then cooled to +10° C. while carrying out an HPLC analysis. The reaction mixture was sequentially washed with 1M aqueous hydrochloric acid (50 ml), 1% aqueous sodium chloride solution (2×25 ml) and a mixture of 1% sodium chloride (25 ml) and saturated sodium bicarbonate (5 ml) solution. The separated organic extract was concentrated in vacuo to give 6.41 g of the desired product as dark brown oil in 101.8% yield. The NMR spectrum showed the presence of residual toluene (8.8%) and starting material (ca 3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247377B2
Source datasetuspto-grants-2012_08
ORD IDord-e145384451e64d6095df34f023666be8
Source noteuspto-grants-2012_08