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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 132816Erstellt: 25. Oktober 2026

1-Bromo-3-chloropropane → 5-(3-Chloro-propoxy)-1H-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/132816

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-3-chloropropaneHCID 8006—
EduktPotassium CarbonateHCID 11430—
EduktEthyl 5-hydroxy-1H-indole-2-carboxylateHCID 90677—
LösungsmittelMethyl Ethyl KetoneHCID 6569—
Produkt5-(3-Chloro-propoxy)-1H-indole-2-carboxylic acid ethyl esterHCID 4511235674%

Reaktionsschritte

A mixture of ethyl-5-hydroxyindole-2-carboxylate (purchased at Biosynth, Ref H-6350, 15 g, 1.0 eq.), 1-bromo-3-chloropropane (8.8 mL, 1.2 eq.) and potassium carbonate (12.12 g, 1.2 eq.) in butanone (200 mL) was stirred 4 days at reflux. The reaction mixture was partitioned between ethyl acetate and water. The aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with water and brine, evaporated in vacuo and purified on silica, eluting with a 19:1 to 2:1 gradient of cyclohexane/ethyl acetate to yield 15.3 g (74%) of the desired product as light yellow solid. MS (m/e): 282.5 (MH+, 100%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07388095B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-f255e45802724c42866eefe1e752fc19
Quellennotizuspto-grants-2008_06