HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15630Erstellt: 24. Oktober 2026
2,3,5-Trimethylphenol → 2-Hydroxy-3,4,6-trimethylbenzaldehyde
https://huagongshe.com/de/reaction/15630
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2,3,5-Trimethylphenol | HCID 12769 | — |
| Edukt | Methane, dichloromethoxy- | HCID 21004 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Katalysator | Titanium Tetrachloride | HCID 24193 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2-Hydroxy-3,4,6-trimethylbenzaldehyde | HCID 11321146 | 40,1% |
Reaktionsschritte
A solution of 2,3,5-trimethylphenol (13.6 g, 100 mmol,) in dichloromethane (20 mL) was ice-cooled, titanium tetrachloride (41.7 g, 220 mmol) was added dropwise over 0.5 hr under nitrogen atmosphere, and the reaction mixture was stirred for 1 hr. Dichloromethyl methyl ether (11.5 g, 100 mmol) was added dropwise, and the mixture was further stirred for 6 hr. The reaction mixture was treated with saturated aqueous ammonium chloride solution, and extracted with dichloromethane. The extract was washed successively with diluted hydrochloric acid, saturated aqueous sodium hydrogencarbonate and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=5:95-50:50) to give the title compound (6.58 g, yield 40%) as pale-brown crystals.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07732626B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-e6060092f6c3494291b7bcca36edccbe |
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| Quellennotiz | uspto-grants-2010_06 |
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