HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1428368Erstellt: 26. Oktober 2026
Triethylamine → 1-Methanesulfonyloxymethyl-cyclopropanecarboxylic acid ethyl ester
https://huagongshe.com/reaction/1428368
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Edukt | Ethyl 1-(hydroxymethyl)cyclopropane-1-carboxylate | HCID 12450336 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1-Methanesulfonyloxymethyl-cyclopropanecarboxylic acid ethyl ester | HCID 57466610 | 94% |
Reaktionsschritte
Triethylamine (5.57 mL, 40.00 mmol) and methanesulfonyl chloride (2.85 mL, 36.60 mmol) were sequentially added to a stirred solution of ethyl 1-(hydroxymethyl)cyclopropanecarboxylate (4.80 g, 33.30 mmol) in dichloromethane (83 mL) at 23° C. The resulting bright yellow solution was stirred at 23° C. for 20 h. The reaction mixture was diluted with water and extracted with dichloromethane. The combined organic layers were dried (MgSO4), filtered, and concentrated to dryness to give the desired product as a brown oil (6.92 g, 94%): 1H NMR (300 MHz, CDCl3) δ 4.33 (s, 2H), 4.16 (q, J=7 Hz, 2H), 3.08 (s, 3H), 1.43 (dd, J=7, 4 Hz, 2H), 1.26 (t, J=7 Hz, 3H), 1.04 (dd, J=7, 4 Hz, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08937083B2 |
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| Quelldatensatz | uspto-grants-2015_01 |
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| ORD ID | ord-95d3ba03b4304c349d5c61f0598d0543 |
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| Quellennotiz | uspto-grants-2015_01 |
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