HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514898Generated: November 3, 2026
3-Chlorobenzotrifluoride → 2-Chloro-6-(trifluoromethyl)benzaldehyde
https://huagongshe.com/reaction/1514898
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chlorobenzotrifluoride | HCID 7374 | — |
| Reactant | Methyl formate | HCID 7865 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-Chloro-6-(trifluoromethyl)benzaldehyde | HCID 17750679 | — |
Reaction Steps
To a solution of 1-chloro-3-trifluoromethylbenzene (1.0 g, 5.54 mmol) in THF (15 mL) cooled to −78° C., under N2 protection was added dropwise n-BuLi (3.81 mL of a 1.6 M solution in hexane, 6.1 mmol). After an hour, formic acid methyl ester (664.8 mg, 11.08 mmol) was added slowly to the solution. After the addition, the solution was warmed to ambient temperature slowly and stirred for 30 min. The reaction mixture was quenched with water and the aqueous layer was extracted with EtOAc. The organic layer was washed with water, brine, dried with MgSO4 and filtered. The solvent was removed under reduced pressure and the residue was purified by flash chromatography using heptane/EtOAc (15:1) as eluent to give 2-chloro-6-trifluoromethylbenzaldehyde as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08222248B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-ecdac2f096c449f8933712c7b067454a |
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| Source note | uspto-grants-2012_07 |
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