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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 261451Erstellt: 26. Oktober 2026

Hydrochloric Acid → 1-(p-Chlorobenzoyl)-2-methyl-5-methoxy-3-indolylacetic acid-ethoxymethyl ester

https://huagongshe.com/reaction/261451

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktIndomethacinHCID 3715—
EduktChloromethyl ethyl etherHCID 18523—
EduktSodium hydrideHCID 24758—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(p-Chlorobenzoyl)-2-methyl-5-methoxy-3-indolylacetic acid-ethoxymethyl esterHCID 2039505271,7%

Reaktionsschritte

To a mixture of 3.6 g of 1-(p-chlorobenzoyl)-2-methyl-5-methoxy-3-indolylacetic acid and 50 ml of dry tetrahydrofuran was added 0.5 g of 50% sodium hydride and the mixture was stirred for 30 minutes. To this mixture was further added 2.5 g of chloromethylethyl ether and the whole was reacted for 3 hours at room temperature. After the reaction was complete, the solvent was removed by distillation under reduced pressure. The residue thus obtained was neutralized with diluted hydrochloric acid, and then extracted with ethyl ether. The ether layer separated was washed with water and dried. The ether was removed by distillation to yield crystals. Recrystallization of the crystals from petroleum ether yielded 3.0 g of 1-(p-chlorobenzoyl)-2-methyl-5-methoxy-3-indolylacetic acid-ethoxymethyl ester as colorless prisms, melting at 60°-61° C. Analysis--Calculated for C22H22ClNO5 : C, 63.48; H, 5.17; N, 3.42. Found: C, 63.53; H, 5.33; N, 3.37.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04165428
Quelldatensatzuspto-grants-1979_08
ORD IDord-444d3cac27454ca8b8c1d3371b66890e
Quellennotizuspto-grants-1979_08