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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006281Generated: October 28, 2026

(Trifluoromethyl)trimethylsilane → HCID 22676779, compound

https://huagongshe.com/reaction/1006281

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 22676821HCID 22676821—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22676779HCID 2267677921%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-(4-methoxyphenyl)-1-{[3-(trifluoromethyl)phenyl]methyl}indole-2-carbaldehyde (Example 218, 200 mg, 0.49 mmol) in tetrahydrofuran (5 mL) was added a 0.5 M solution of TMSCF3 in tetrahydrofuran (4.9 mL, 2.4 mmol). The resulting solution was cooled to 0° C. and a 1.0 M solution of TBAF in tetrahydrofuran (0.10 mL, 0.10 mmol) was added. The mixture was stirred for 10 min at 0° C. and then let warm to RT and quenched by the addition of water. The resulting mixture was extracted with tetrahydrofuran, adsorbed onto silica, and purified by flash chromatography on silica in 4:1 hexane:ethyl acetate (v/v) to yield 49 mg (21%) of an orange solid. 1H NMR (300 MHz, DMSO-d6) δ 7.60-7.26 (m, 6H), 7.22-7.01 (m, 6H), 5.81 (s, 2H), 3.83 (s, 3H); mass spectroscopy gave MH+=480.2 (calc'd exact mass for C25H19F3NO2=479.13).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787651B2
Source datasetuspto-grants-2004_09
ORD IDord-03b5349e0c5a4aceaf083bf4ad7179cc
Source noteuspto-grants-2004_09