Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36923Erstellt: 24. Oktober 2026

3',4'-Dimethoxycinnamic acid → 3,4-Dimethoxycinnamoylchloride

https://huagongshe.com/de/reaction/36923

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3',4'-Dimethoxycinnamic acidHCID 16848—
EduktOxalyl chlorideHCID 65578—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3,4-DimethoxycinnamoylchlorideHCID 53399206—

Reaktionsschritte

To a mixture of 3,4-dimethoxycinnamic acid (540 mg), DMF (2 drops) and tetrahydrofuran (10 ml) was added oxalyl chloride (0.27 ml) dropwise. The mixture was stirred at room temperature for 40 minutes, at the end of which time the solvent was distilled off to give 3,4-dimethoxycinnamoyl chloride. The chloride was dissolved in dichloromethane (10 ml) followed by addition of 3-amino-4-(2-methylphenyl)-7,8-dihydrocyclopenta [g] [1]benzopyran-2(6H)-one (582 mg) and N,N-dimethylaniline (0.25 ml). The mixture was then stirred at room temperature for 20 hours, after which it was washed with water, dried (MgSO4) and distilled to remove the solvent. The residue was chromatographed on silica gel and eluted with benzene-acetone (9:1) to give 3-(3,4-dimethoxycinnamoylamino) -4-(2-methylphenyl)-7,8-dihydrocyclopenta[g] 1benzopyran-2(6H)-one as oil. The oil was crystallized from ethanol-isopropyl ether (648 mg, 67.4%). Recrystallization from acetone gave colorless needles, m.p. 159°-160° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05418239
Quelldatensatzuspto-grants-1995_05
ORD IDord-03af43923d334bb58f46283316bba5de
Quellennotizuspto-grants-1995_05