HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894708Generated: October 29, 2026
Sulfuric Acid → 2,6-Difluoro-4-methylbenzaldehyde
https://huagongshe.com/reaction/1894708
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 3,5-Difluorotoluene | HCID 2778329 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,6-Difluoro-4-methylbenzaldehyde | HCID 21063800 | 90% |
Reaction Steps
To a solution of 1,3-difluoro-5-methylbenzene (10.2 g, 80 mmol) in anhydrous ether (80 mL) was added n-BuLi (2.5 M solution in hexane, 48 ml, 120 mmol) over a 20 min period while the internal temperature was maintained at around −50° C. After stirring at that temperature for 1.5 hr, DMF (14.6 g, 200 mmol) was added over a 20 min period. After stirring at the same temperature for an additional 1.5 h, the reaction mixture was slowly poured into 1N aqueous sulfuric acid (300 mL) and extracted with ether three times. The combined organic layers were washed with brine, dried over anhydrous MgSO4, filtered and concentrated to give the title compound (11.2 g, 90%). 1H-NMR (500 MHz, CDCl3): δ 10.25 (s, 1H), 6.75 (d, 2H, J=9.9 Hz), 2.39 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513289B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-23bc24ceced04c108cf320aea6277d2c |
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| Source note | uspto-grants-2013_08 |
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