HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005490Generated: October 30, 2026
Sulfuric Acid → 2,3-Difluoro-6-trifluoromethylbenzaldehyde
https://huagongshe.com/reaction/1005490
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2,3-Difluoro-6-(trifluoromethyl)benzonitrile | HCID 10104456 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,3-Difluoro-6-trifluoromethylbenzaldehyde | HCID 10998287 | — |
Reaction Steps
2.0 g of 2,3-difluoro-6-trifluoromethylbenzonitrile was dissolved in 20 ml of anhydrous dichloromethane and the resultant solution was cooled down to -78° C. under a nitrogen atmosphere. To the solution was then gradually added dropwise with 7.1 ml of 1.5 M toluene solution of diisobutyl aluminium hydride (DIBAL) over 30 minutes. After stirring the solution at -78° C. for 1 hour, the solution was allowed to room temperature. The solution was then added with 7 ml of saturated aqueous solution of ammonium chloride, stirred for 30 minutes and subsequently added with 33 ml of 5% sulfuric acid. The mixture was then extracted with ether, and the organic layer obtained was washed with saturated saline solution and was then dried over anhydrous magnesium sulfate. After a process for the concentration, the organic solution was purified by using silica gel column chromatography to obtain 1.36 g of the title compound (nD 20.6-1.4357).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06054605 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-7ae59446d3a04adf955b8cff466a5489 |
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| Source note | uspto-grants-2000_04 |
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