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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458903Generated: October 29, 2026

Tetrahydrofuran → HCID 73445535, compound

https://huagongshe.com/reaction/458903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-Chloro-5-(trifluoromethyl)benzaldehydeHCID 688181—
CatalystZincchlorideHCID 3007855—
CatalystZinc bromideHCID 10421208—
SolventDiethylether waterHCID 21584184—
ProductHCID 73445535HCID 73445535—

Reaction Conditions

Temperature10 °C

Reaction Steps

To a solution of 2-chloro-5-trifluoromethylbenzaldehyde (300 mg) in 5 mL THF was added 40 mg of ZnBr2. With stirring, 360 mg of α,α-bis(trimethylsilyl)-t-butylacetaldimine (7) was added, and stirring was continued overnight. The solution was cooled to 10° C., then hydrolyzed by the addition of a solution of ZnCl2 (40 mg) in diethyl ether/water (3 mL each), followed by stirring at room temperature for 1 h. The solids were removed by filtration through Celite and the filtrate extracted with diethyl ether (2×). The combined ether extracts were washed with water and brine, dried over magnesium sulfate, filtered and concentrated to provide the title compound as a light brown oil (220 mg): 1H NMR (CDCl3) δ 6.09 (s, 2H), 6.14 (s, 1 H), 6.86–6.98 (m, 4 H), 7.43 (d, 1 H, J=9.6 Hz), 9.69 (d, 1 H, J=4.5 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192976B2
Source datasetuspto-grants-2007_03
ORD IDord-603039915d254bc08713d04064c3abf9
Source noteuspto-grants-2007_03