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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607251Generated: October 30, 2026

Trifluoroacetic acid → Trifluoroacetic acid

https://huagongshe.com/reaction/607251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPentamethylbenzeneHCID 12784—
ReactantHCID 66808430HCID 66808430—
ProductTrifluoroacetic acidHCID 642247%
ProductHCID 60204799HCID 60204799—

Reaction Steps

A solution of the product from Example 147D (38.8 mg, 0.059 mmol) and pentamethylbenzene (87 mg, 0.5901 mmol) in trifluoroacetic acid (5 mL) was stirred at room temperature for 2 hours. The solvent was removed by rotary evaporation under vacuum and co-evaporated with methylene chloride/hexanes (2×). The resulting solid was triturated with hexanes (3×) and purified by HPLC with TFA to provide the title compound as a trifluoroacetic acid salt (22 mg, 47%). 1H NMR (300 MHz, DMSO-D6) δ ppm: 1.36 (d, J=6.99 Hz, 6H), 3.20-3.39 (m, 1H), 6.78 (d, J=8.82 Hz, 2H), 6.95 (d, J=9.19 Hz, 2H), 7.02 (d, J=8.82 Hz, 1H), 7.36 (dd, J=8.64, 2.02 Hz, 1H), 7.55 (d, J=8.46 Hz, 1H), 7.78 (d, J=1.47 Hz, 1H), 7.91 (d, J=8.82 Hz, 1H), 8.11 (dd, J=8.64, 2.02 Hz, 1H), 8.35 (d, J=1.84 Hz, 1H), 8.94 (s, 1H), 9.03 (d, J=8.82 Hz, 1H), 9.46 (br s, 1H), 11.63 (br s, 1H); MS (APCI+) m/z 567/569 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915411B2
Source datasetuspto-grants-2011_03
ORD IDord-4cb8959d22fb41be937fe2bb25e45686
Source noteuspto-grants-2011_03