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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486836Generated: October 31, 2026

Trifluoroacetic acid → HCID 23135633, compound

https://huagongshe.com/reaction/1486836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 81697470HCID 81697470—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 23135633HCID 2313563384%

Reaction Steps

To a solution of (4-bromo-3-(trifluoromethyl)phenyl)(phenyl)methanol (168 mg, 0.507 mmol) in 0.34 mL of anhydrous DCM (C=1.5M), were successively added dropwise trifluoroacetic acid (195 μL, 5 eq) and triethylsilane (243 μL, 3 eq). After 1 h45 of stirring at r.t., the reaction mixture was hydrolyzed with a saturated NH4Cl solution (5 mL). The layers were diluted with 20 mL of DCM and 20 mL of water and then separated. The aqueous layer was extracted with DCM (3×10 mL) The combined organic phase was washed with a saturated NaHCO3 solution (20 mL), brine (20 mL), dried over MgSO4, filtered and concentrated in vacuo. The crude residue was purified by silica gel flash chromatography (cyclohexane) to afford the desired product in 84% yield (135 mg) as uncoloured oil. 1H NMR (300 MHz, CDCl3) δ 7.62 (d, J=8.2 Hz, 1H), 7.54 (d, J=2.0 Hz, 1H), 7.34 (tt, J=7.9, 1.8 Hz, 2H), 7.26 (t, J=7.3 Hz, 1H), 7.22-7.15 (m, 3H), 4.00 (s, 2H); 13C NMR (75 MHz, CDCl3) δ 141.0 (C), 139.5 (C), 135.1 (CH), 133.6 (CH), 130.2 (q, J=31.3 Hz, C), 129.0 (CH), 128.9 (CH), 128.4 (q, J=5.4 Hz, CH), 126.8 (CH), 123.1 (q, J=273.4 Hz, C), 117.5 (q, J=1.9 Hz, C), 41.3 (CH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428500B2
Source datasetuspto-grants-2016_08
ORD IDord-8c7445e2ca4c4007aa74d712359e4059
Source noteuspto-grants-2016_08