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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1533055Erstellt: 25. Oktober 2026

Oxalyl chloride → 2,3-Dihydro-1-benzofuran-7-carbonyl chloride

https://huagongshe.com/reaction/1533055

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxalyl chlorideHCID 65578—
Edukt2,3-Dihydro-1-benzofuran-7-carboxylic acidHCID 2795014—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt2,3-Dihydro-1-benzofuran-7-carbonyl chlorideHCID 279501698,9%

Reaktionsschritte

2,3-Dihydrobenzo[b]furan-7-oic acid (3 g) (see Preparation 32) was suspended in anhydrous dichloromethane (30 ml) and oxalyl chloride (3.5 g) added, followed by addition of dimethylformamide (3 drops). The mixture was stirred at room temperature for 2.5 hours, the solvent then removed under reduced pressure, the resulting residue dissolved in dichloromethane and the solvent removed under reduced pressure. The residue was again dissolved in dichloromethane and the solvent removed under reduced pressure to give 2,3-dihydrobenzo[b]furan-7-oyl chloride as a pink solid (3.3 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06207678B1
Quelldatensatzuspto-grants-2001_03
ORD IDord-9642afae95fe480ab07f43aa4726d067
Quellennotizuspto-grants-2001_03