HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458903Generated: October 29, 2026
Tetrahydrofuran → HCID 73445535, compound
https://huagongshe.com/reaction/458903
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Chloro-5-(trifluoromethyl)benzaldehyde | HCID 688181 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Catalyst | Zinc bromide | HCID 10421208 | — |
| Solvent | Diethylether water | HCID 21584184 | — |
| Product | HCID 73445535 | HCID 73445535 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192976B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-603039915d254bc08713d04064c3abf9 |
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| Source note | uspto-grants-2007_03 |
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