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HRID 2068548Erstellt: 26. Oktober 2026

Triethylamine → Ethyl 1-(4-cyclopropoxybenzamido)cyclopropanecarboxylate

https://huagongshe.com/reaction/2068548

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
EduktEthyl 1-aminocyclopropane-1-carboxylate hydrochlorideHCID 386203—
Edukt4-Cyclopropoxybenzoic acidHCID 21452864—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktEthyl 1-(4-cyclopropoxybenzamido)cyclopropanecarboxylateHCID 6723442785%

Reaktionsschritte

To a 0° C. suspension of 4-cyclopropoxybenzoic acid (24.5 g, 137.3 mmol) in dichloromethane (350 mL) containing 2 drops of DMF, slowly add oxalyl chloride (23.8 mL, 274.7 mmol). After addition, remove the cooling bath and stir for 2 hours. Concentrate the material to dryness under reduced pressure. Dissolve the residue in dichloromethane (500 mL), and then add ethyl 1-aminocyclopropanecarboxylate hydrochloride (Indofine #04-265, 24.9 g, 150.5 mmol) and triethylamine (57.2 mL, 410.4 mmol). Stir the mixture at ambient temperature for approximately 16 hours. Wash the mixture once with 10% NaHSO4 (250 mL). Separate the organic portion and extract the aqueous portion 2× with dichloromethane (200 mL). Combine the organic, dry over sodium sulfate, filter, and concentrate under reduced pressure. Purify the crude mixture by flash chromatography (0% to 45% EtOAc/Hex) to give the title compound (33.7 g, 85%): MS (m/z): 290 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08299061B2
Quelldatensatzuspto-grants-2012_10
ORD IDord-66cf8552de9a4129b5ce6d2444e291c0
Quellennotizuspto-grants-2012_10