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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Chloromethyl 2-(trimethylsilyl)ethyl ether | HCID 2724271 | — |
| Reactant | 1-[3,5-Bis(trifluoromethyl)phenyl]ethane-1,2-diol | HCID 22293512 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,5-Bis(trifluoromethyl)-alpha-{[2-(trimethylsilyl)ethoxy]methoxymethyl}benzenemethanol | HCID 86590361 | 49% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06953792B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-26ef180a91d445458ac6694f42f4c006 |
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| Source note | uspto-grants-2005_10 |
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