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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042330Generated: November 2, 2026

Potassium Carbonate → HCID 59133208, compound

https://huagongshe.com/reaction/2042330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
Reactant2-(Trifluoromethyl)benzenethiolHCID 2777889—
SolventAcetoneHCID 180—
ProductHCID 59133208HCID 59133208—

Reaction Conditions

Temperature45 °C

Reaction Steps

To a stirred solution of 2-(trifluoromethyl)benzenethiol (5.000 g, 0.028 mol) in acetone (50 mL) was added 2-bromo-1,1-diethoxyethane (6.08 g, 0.030 mol) and potassium carbonate (7.757 g, 0.056 mol). The resulting mixture was then stirred at 45° C. for 2 hours prior to removal of the solvent in vacuo and suspension of the residue in EtOAc. The inorganic salts were filtered off and the organic phase was concentrated to give crude product, which was used in next step without further purification. This residue was dissolved in toluene (50 mL), and to this solution was added PPA (10 g) and the resulting mixture stirred at 95-100° C. for 2 hours. The mixture was allowed to cool to rt, was poured into ice-water, then extracted with EtOAc (3×50 mL). The combined extracts were washed with aqueous sodium bicarbonate followed by brine, then dried over anhydrous sodium sulfate and evaporated under reduced pressure to yield an oil. This was purified by column chromatography over silica gel eluting with hexane to give 7-trifluoromethyl-benzo[b]thiophene. 1H NMR (400 MHz, MeOD) δ ppm 7.49-7.57 (m, 2H), 7.70 (d, J=7.33 Hz, 1H), 7.74 (d, J=5.56 Hz, 1H) and 8.10 (d, J=8.08 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586546B2
Source datasetuspto-grants-2013_11
ORD IDord-915c2c6cc7f14c438234e4420306c018
Source noteuspto-grants-2013_11