HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415998Generated: October 26, 2026
Water → 4-Bromo-2-(trifluoromethyl)benzaldehyde
https://huagongshe.com/reaction/415998
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Benzene, 4-bromo-1-(dibromomethyl)-2-(trifluoromethyl)- | HCID 59474514 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Bromo-2-(trifluoromethyl)benzaldehyde | HCID 12187218 | 81% |
Reaction Steps
Combine 4-bromo-1-(dibromomethyl)-2-(trifluoromethyl)benzene (6.66 g, 16.8 mmol), silver nitrate (14.8 g, 87.3 mmol), THF (250 mL), and water (35 mL) in a 500 mL flask equipped with a magnetic stir bar, reflux condenser, and N2 inlet. Reflux the mixture while stirring for 2.5 hours then cool to room temperature. Filter the reaction through Celite®, add ethyl acetate (250 mL) and wash with water (2×200 mL) then saturated aqueous sodium chloride solution (1×200 mL). Dry over anhydrous magnesium sulfate, concentrate to an orange oil, and purify the crude product via silica gel chromatography eluting with hexanes to afford 3.46 g (81%) of the product as a clear oil: 1H NMR (300 MHz, CDCl3) δ 10.35-10.33 (m, 1H), 8.0 (d, 1H, J=8.3 Hz), 7.93 (d, 1H, J=1.4 Hz), 7.86 (dd, 1H, J=1.2 Hz, J=8.3 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088776B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-4ce2748c2c844cc4a61beb76d4189b03 |
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| Source note | uspto-grants-2012_01 |
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