HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21256Erstellt: 24. Oktober 2026
Chloromethyl Methyl Ether → 3-Chloro-4-methoxymethoxybenzoic acid
https://huagongshe.com/de/reaction/21256
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chloromethyl Methyl Ether | HCID 7864 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 3-Chloro-4-hydroxybenzoic acid | HCID 19860 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 3-Chloro-4-methoxymethoxybenzoic acid | HCID 57986688 | 95,1% |
Reaktionsschritte
3-Chloro-4-hydroxybenzoic acid 0.5 hydrate (2.00 g, 11.6 mmol) was suspended in dichloromethane (50 mL), and the suspension was added with diisopropylethylamine (8.10 mL, 46.5 mmol) and chloromethyl methyl ether (1.80 mL, 23.7 mmol), under ice-cooling. The reaction mixture was warmed to room temperature and stirred for 1.5 hours. The reaction mixture was added with chloromethyl methyl ether (0.45 mL, 5.92 mmol) under ice-cooling, and stirred at room temperature for 1.5 hours. The reaction mixture was added with methanol (100 mL) and 4 mol/L aqueous potassium hydroxide solution (50 mL) and stirred at room temperature for 18 hours. The solvent was evaporated under reduced pressure, and the residue was added with 4 mol/L hydrochloric acid and water, followed by extracting with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to obtain 3-chloro-4-methoxymethoxybenzoic acid (2.39 g, yield 95%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07745641B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-98ca684b2d7041bc8d3afabb280632b7 |
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| Quellennotiz | uspto-grants-2010_06 |
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