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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966967Generated: October 30, 2026

Water → 3,5-Bis(trifluoromethyl)-alpha-{[2-(trimethylsilyl)ethoxy]methoxymethyl}benzenemethanol

https://huagongshe.com/reaction/966967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
Reactant1-[3,5-Bis(trifluoromethyl)phenyl]ethane-1,2-diolHCID 22293512—
SolventDichloromethaneHCID 6344—
Product3,5-Bis(trifluoromethyl)-alpha-{[2-(trimethylsilyl)ethoxy]methoxymethyl}benzenemethanolHCID 8659036149%

Reaction Steps

N-Ethyl-N,N-diisopropylamine (465 μl, 2.67 mmol) was added over 2 minutes, to a solution of (RS)-1-[3,5-bis(trifluoromethyl)phenyl]-1,2-ethanediol (Description 3, 488 mg, 1.78 mmol) and [2-(chloromethoxy)ethyl]trimethylsilane (315 μl, 1.78 mmol) in dichloromethane (3 mL) and the mixture was stirred at room temperature for 4 hours, then at 50° C. for 1 hour. The mixture was cooled and dichloromethane (20 mL) and water (20 mL) were added. The layers were separated and the aqueous layer was extracted with dichloromethane (10 mL). The combined organic fractions were dried (Na2SO4) and the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with isohexane/EtOAc (90:10) to give the title compound (352 mg, 49%). 1H NMR (400 MHz, CDCl3) δ 7.86 (2H, s), 7.79 (1H, s), 4.96 (1H, m), 4.73 (2H, s), 3.87 (1H, dd, J 11.1, 3.0 Hz), 3.73 (1H, br s), 3.61 (3H, m), 0.93 (2H, t, J 8.5 Hz), and 0.02 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06953792B2
Source datasetuspto-grants-2005_10
ORD IDord-26ef180a91d445458ac6694f42f4c006
Source noteuspto-grants-2005_10