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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 220777Erstellt: 27. Oktober 2026

Acetic Acid → 1-Tosyl-3,4-dihydro-1H-benzo[b]azepin-5(2H)-one

https://huagongshe.com/reaction/220777

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktHydrochloric AcidHCID 313—
Eduktethyl 5-hydroxy-1-tosyl-2,3-dihydro-1H-benzo[b]azepine-4-carboxylateHCID 54718720—
Edukt5-hydroxy-1-(toluene-4-sulfonyl)-2,3-dihydro-1H-benzo[b]azepine-4-carboxylic acid methyl esterHCID 57555388—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt1-Tosyl-3,4-dihydro-1H-benzo[b]azepin-5(2H)-oneHCID 26685260%

Reaktionsschritte

A mixture of 5-hydroxy-1-(toluene-4-sulfonyl)-2,3-dihydro-1H-benzo[b]azepine-4-carboxylic acid methyl ester and 5-hydroxy-1-(toluene-4-sulfonyl)-2,3-dihydro-1H-benzo[b]azepine-4-carboxylic acid ethyl ester from Example E5.3 were heated at reflux in a mixture of ethanol (100 ml), acetic acid (300 ml), concentrated HCl (100 ml) and water (50 ml) for 18 h. The mixture was cooled to room temperature, diluted with water (800 ml) and extracted with chloroform. The combined organic ex-tracts were dried, filtered and reduced in vacuo. The residue was crystallised twice from methanol to yield the title compound (44 g, 60% over two steps).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202858B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-e70ace56b00e42cb9b06c565f7e98394
Quellennotizuspto-grants-2012_06