HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428025Generated: October 25, 2026
p-Toluenesulfonic acid → 2-Bromo-1-(diethoxymethyl)-4-fluorobenzene
https://huagongshe.com/reaction/428025
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | 2-Bromo-4-fluorotoluene | HCID 74016 | — |
| Reactant | 2-Bromo-4-fluorobenzaldehyde | HCID 2773319 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | 2-Bromo-1-(diethoxymethyl)-4-fluorobenzene | HCID 18357605 | — |
Reaction Steps
To a solution of 6.5 g of 2-bromo4-fluoro-benzaldehyde (prepared by the oxidation of 2-bromo-4-fluoro-toluene by the method reported by V. J. Bauer, B. J. Duffy, D. Hoffman, S. S. Klioze, R. W. Kosley, Jr., A. R. McFadden, L. L. Martin, H. H. Ong and H. M. Geyer III, J. Med. Chem., 1976, 19, 1315) in 25 ml of ethanol was added triethylorthoformate followed by 0.05 g of p-toluene sulfonic acid. The solution was stirred at room temperature for 2.25 h then diluted with 100 ml of a 5% sodium carbonate solution and extracted with two 100 ml portions of ether. The combined organic layers were washed with 50 ml of brine and dried over sodium sulfate. Evaporation of the solvent yielded 8.8 g of 2-bromo4-fluoro-benzaldehyde diethyl acetal as an oil, 1H NMR (200 MHz; CDCl3) δH 5.60 (CHO3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06313139B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-004b082d24bb459191da304bdf2ad281 |
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| Source note | uspto-grants-2001_11 |
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