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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1428368Erstellt: 26. Oktober 2026

Triethylamine → 1-Methanesulfonyloxymethyl-cyclopropanecarboxylic acid ethyl ester

https://huagongshe.com/reaction/1428368

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
EduktEthyl 1-(hydroxymethyl)cyclopropane-1-carboxylateHCID 12450336—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-Methanesulfonyloxymethyl-cyclopropanecarboxylic acid ethyl esterHCID 5746661094%

Reaktionsbedingungen

Temperatur23 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08937083B2
Quelldatensatzuspto-grants-2015_01
ORD IDord-95d3ba03b4304c349d5c61f0598d0543
Quellennotizuspto-grants-2015_01