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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 551861Erstellt: 26. Oktober 2026

Oxalyl chloride → 4,5,6,7-Tetrahydro-benzo[b]thiophene-2-carbonyl chloride

https://huagongshe.com/reaction/551861

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxalyl chlorideHCID 65578—
Edukt4,5,6,7-Tetrahydro-1-benzothiophene-2-carboxylic acidHCID 2063443—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt4,5,6,7-Tetrahydro-benzo[b]thiophene-2-carbonyl chlorideHCID 6485362—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

4,5,6,7-Tetrahydro-benzo[b]thiophene-2-carboxylic acid (1.0 g, 5.50 mmol) is dissolved in dichloromethane [DCM] (25 mL) that contains 5 drops of N,N-dimethylformamide [DMF] under nitrogen and cooled to 0° C. Oxalyl chloride (13.7 mL of a 2.0M solution in DCM) is added via syringe and allowed to warm to RT over 1 hour. All solvent is then removed under reduced pressure, and the resultant oil is reduced from toluene (3×20 mL) to remove residual oxalyl chloride. The residue is then dissolved in ethyl acetate and washed with saturated sodium bicarbonate (1×100 mL), then washed with saturated sodium chloride (1×100 mL) and dried over sodium sulfate. The solution is then filtered and concentrated under reduced pressure to give 4,5,6,7-tetrahydro-benzo[b]thiophene-2-carbonyl chloride (1) as an off-white solid (1.03 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07947835B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-0f89938f0f464b328e205671582d1545
Quellennotizuspto-grants-2011_05