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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006292Generated: November 2, 2026

Triacetoxyperiodinane → HCID 22676761, compound

https://huagongshe.com/reaction/1006292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantHCID 22676779HCID 22676779—
SolventDichloromethaneHCID 6344—
ProductHCID 22676761HCID 2267676170.7%

Reaction Steps

Dess-Martin reagent (39 mg, 0.09 mmol) was added to a stirred solution of 2,2,2-trifluoro-1-(3-(4-methoxphenyl)-1-{[3-(trifluoromethyl)phenyl]methyl}indol-2-yl)ethan-1-ol (Example 219, 40 mg, 0.08 mmol) in dichloromethane (2 mL). The resulting solution was stirred for 2 hours, more oxidant was added, and then the mixture was left stirring for 18 h. The reaction was quenched with a mixed aqueous solution of saturated sodium bicarbonate and saturated sodium thio sulfate (1:1, 10 mL), and the mixture was extracted with ethyl acetate (2×10 mL). The combined organic extracts were washed with water, and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo. Silica gel flash chromatography using hexane/ethyl acetate (4/1) as the eluant gave 2,2,2-trifluoro-1-(3-(4-methoxyphenyl)-1-{[3-(trifluoromethyl)phenyl]methyl}indol-2-yl)ethan-1-one as an orange oil (27 mg, 70%): 1H NMR (300 MHz, DMSO-d6) δ 7.76 (d, 1H), 7.47-7.62 (m, 4H), 7.20-7.45 (m, 5H), 7.05 (d, 2H), 5.76 (s, 2H); MS (MH+) calcd for C25H18F6NO2: 478., found: 478.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787651B2
Source datasetuspto-grants-2004_09
ORD IDord-02b0891f0ecc4a1e85b85347fb2eec62
Source noteuspto-grants-2004_09