HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485068Generated: October 31, 2026
Hydrochloric Acid → 4-(1,1-Difluoroethyl)benzaldehyde
https://huagongshe.com/reaction/1485068
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Bromo-4-(1,1-difluoroethyl)benzene | HCID 45158847 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Butyllithium | HCID 178418339 | — |
| Product | 4-(1,1-Difluoroethyl)benzaldehyde | HCID 20387577 | — |
Reaction Steps
To a solution of 1-bromo-4-(1,1-difluoroethyl)benzene (1.00 g) in tetrahydrofuran (10.0 mL), n-butyl lithium (2.69 mol/L, solution in n-hexane, 1.68 mL) was added at −80° C. and the mixture was stirred at that temperature for 5 minutes. Subsequently, N,N-dimethylformamide (0.522 mL) was added at −80° C. and after stirring the mixture at that temperature for 20 minutes, 2 mol/L hydrochloric acid (2.50 mL) was added. After bringing the reaction mixture to room temperature, two extractions were conducted with ethyl acetate and the combined organic layers were washed with water. After drying over anhydrous magnesium sulfate and the desiccant was removed by filtration; the filtrate was then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=100:0-90:10) to give the titled compound as a colorless oil (510 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422240B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-e0350786af7147eab5fffba7ba6000bb |
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| Source note | uspto-grants-2016_08 |
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