Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1109766Erstellt: 25. Oktober 2026

Ethyl 7-hydroxychromane-2-carboxylate → Benzenemethanol, 3-(2-quinolinylmethoxy)-

https://huagongshe.com/reaction/1109766

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 7-hydroxychromane-2-carboxylateHCID 11085381—
Edukt(3-Sulfanylphenyl)methanolHCID 12813879—
EduktBenzothiazole, 2-(chloromethyl)-5-fluoro- (9CI)HCID 14204210—
Edukt2-Ethoxycarbonyl-7-(5-fluorobenzothiazol-2-ylmethoxy)chromanHCID 19019503—
Edukt3-(5-Fluorobenzothiazol-2-ylmethylthio)benzyl alcoholHCID 53906810—
ProduktBenzenemethanol, 3-(2-quinolinylmethoxy)-HCID 14650410—

Reaktionsschritte

In a similar manner 4-(5-fluorobenzothiazol-2-ylmethoxy)-4'-hydroxydiphenyl, m.p. 210°-211° C. was prepared from 2-chloromethyl-5-fluorobenzothiazole and 4,4-dihydroxydiphenyl, 3-(5-fluorobenzothiazol-2-ylmethylthio)benzyl alcohol was prepared from 3-mercaptobenzyl alcohol and 2-chloromethyl-5-fluorobenzothiazole and 2-ethoxycarbonyl-7-(5-fluorobenzothiazol-2-ylmethoxy)chroman, m.p. 109°-112° C. was prepared from 2-chloromethyl-5-fluorobenzothiazole and 2-ethoxycarbonyl-7-hydroxychroman.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05322847
Quelldatensatzuspto-grants-1994_06
ORD IDord-0fd36c46502342dcac32194ed747c110
Quellennotizuspto-grants-1994_06