HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1247670Erstellt: 26. Oktober 2026
2-Ethylphenol → Ethyl 2-(4-(chlorosulfonyl)-2-ethylphenoxy)acetate
https://huagongshe.com/reaction/1247670
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Ethylphenol | HCID 6997 | — |
| Edukt | Ethyl bromoacetate | HCID 7748 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Chlorosulfonic acid | HCID 24638 | — |
| Lösungsmittel | Methyl Ethyl Ketone | HCID 6569 | — |
| Produkt | Ethyl 2-(4-(chlorosulfonyl)-2-ethylphenoxy)acetate | HCID 21986343 | — |
Reaktionsschritte
A solution of 2-ethylphenol (24.4 g, 200 mmol), potassium carbonate (41.4 g, 300 mmol) and ethyl bromoacetate (36.7 g, 220 mmol) in 2-butanone (250 ml) was stirred at 100° C. for 24 h. The reaction mixture was filtered and evaporated. The residue was dissolved in benzol (100 ml), washed with sodium carbonate solution (5%, 25 ml), dried and evaporated. The residue was dissolved in dichloromethane (100 ml) and chlorosulfonic acid (34.9 g, 300 mmol) was added slowly at −5° C. The reaction mixture was stirred at room temperature for 6 h. Ice water (25 ml) was added and the mixture was extracted with dichloromethane (3×100 ml). The combined organic phases were washed with water, dried and evaporated to give crude (4-chlorosulfonyl-2-ethyl-phenoxy)-acetic acid ethyl ester as an oil. Crystallization from heptane (500 ml) gave the desired product in 31.6 g (52%) yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07129268B2 |
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| Quelldatensatz | uspto-grants-2006_10 |
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| ORD ID | ord-9993f774f44340da8254cc5e0e0adc18 |
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| Quellennotiz | uspto-grants-2006_10 |
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