HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284911Generated: November 1, 2026
Sulfuric Acid → o-(Trifluoromethyl)benzaldehyde
https://huagongshe.com/reaction/1284911
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Benzene, 1-bromo-2-(trifluoromethyl)- | HCID 9806 | — |
| Reactant | N-Methylformanilide | HCID 66737 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | o-(Trifluoromethyl)benzaldehyde | HCID 123067 | 68.3% |
Reaction Steps
2.8 Grams of metallic magnesium, 25 g of 2-bromo-α,α,α-trifluorotoluene and 120 ml of ether were reacted to prepare a Grignard ragent by a conventional method, then 15 g of N-methylformanilide were added dropwise thereto, and the reaction mixture was allowed to stand for 3 hours. Under an ice-cooled condition, a dilute sulfuric acid was added to the reaction mixture. The ethereal layer was separated and was washed with a saturated sodium chloride aqueous solution and with a saturated sodium hydrogencarbonate aqueous solution, then was dried with anhydrous sodium sulfate, and was concentrated. The residue was purified by distillation under reduced pressure to yield 13.2 g of 2-trifluoromethylbenzaldehyde. Boiling point: 62°-65° C. (at 17 mm-Hg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04564619 |
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| Source dataset | uspto-grants-1986_01 |
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| ORD ID | ord-9d544515277c4b0d813d4a207c38c1e9 |
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| Source note | uspto-grants-1986_01 |
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