HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969449Generated: October 30, 2026
Acetic Acid → 3-(1,1-difluoroethyl)benzaldehyde
https://huagongshe.com/reaction/1969449
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | 3-(1,1-Difluoroethyl)benzonitrile | HCID 22261681 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(1,1-difluoroethyl)benzaldehyde | HCID 57471637 | — |
Reaction Steps
Dissolve 3-(1,1-difluoro-ethyl)-benzonitrile (4.39 g, 26.26 mmol) in toluene (44 mL). Place the reaction under nitrogen, cool to −78° C. in a dry-ice bath, then add diisobutylaluminum hydride (52.5 mmol, 1 M solution in toluene) dropwise over 30 minutes with stirring. Stir the reaction in the dry-ice bath for 30 minutes, then add glacial HOAc (14 mL) dropwise to control foaming, followed by water (100 mL). Stir the reaction mixture overnight at room temperature. Separate the layers; extract the cloudy aqueous with toluene. Wash the toluene extracts with brine, dry the organics over magnesium sulfate, filter, and evaporate to afford 3-(1,1-difluoro-ethyl)-benzaldehyde as a pale yellow oil. (4.0 g, 90%). 1H NMR (400 MHz, CDCl3): δ 10.03 (s, 1H), 8.00 (s, 1H), 7.92 (d, J=7.5 Hz, 1H), 7.75 (d, J=7.5 Hz, 1H), 7.58 (t, J=7.7 Hz, 1H), 1.98-1.89 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08426448B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-9198519df8084be299b5770a23d950f6 |
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| Source note | uspto-grants-2013_04 |
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