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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 493492Erstellt: 25. Oktober 2026

1-benzyl-1H-indole-3-carboxylic acid → 1-benzylindole-3-carbonyl Chloride

https://huagongshe.com/reaction/493492

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-benzyl-1H-indole-3-carboxylic acidHCID 33671—
EduktOxalyl chlorideHCID 65578—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-benzylindole-3-carbonyl ChlorideHCID 10492228—

Reaktionsschritte

Oxalyl chloride (7.1 mL, 81.4 mmol) was added under nitrogen dropwise over 10 minutes to a suspension of 1-benzyl-1H-indole-3-carboxylic acid (4.10 g, 16.3 mmol) in 200 mL of methylene chloride at room temperature. When the oxalyl chloride was added there was an immediate evolution of gas and within 30 minutes all of the solid had dissolved. After the addition of the oxalyl chloride the reaction was stirred at room temperature for 2 h. The solvent and excess oxalyl chloride were removed under reduced pressure. The residue was taken up in benzene and then concentrated to dryness under reduced pressure to give 1-benzyl-1H-indole-3-carbonyl chloride, which was used in the following reaction without purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07534894B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-077fa6822c9143789210fa82aad8b7a5
Quellennotizuspto-grants-2009_05