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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1109765Erstellt: 24. Oktober 2026

3-Hydroxybenzyl alcohol → 2,7-Naphthalenediol

https://huagongshe.com/de/reaction/1109765

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Hydroxybenzyl alcoholHCID 102—
Edukt2-(Chloromethyl)-5-(trifluoromethyl)-1,3-benzothiazoleHCID 14204205—
EduktHCID 53867966HCID 53867966—
Produkt2,7-NaphthalenediolHCID 11397—
Produkt2-(Chloromethyl)-6-fluoroquinolineHCID 11241007—
ProduktBenzothiazole, 2-(chloromethyl)-5-fluoro- (9CI)HCID 14204210—
ProduktHCID 19019454HCID 19019454—

Reaktionsschritte

In a similar manner, starting with 2-chloromethyl-5-trifluoromethylbenzothiazole and 3-hydroxy benzyl alcohol and following this procedure, 3-(5-trifluoromethylbenzothiazol-2-ylmethoxy)benzyl alcohol was prepared, m.p. 117°-119° C., 2-chloromethyl-5-fluorobenzothiazole and 2,7-dihydroxynaphthalene gave 2-(5-fluorobenzothiazol-2-ylmethoxy)-7-hydroxynaphthalene, m.p. 218°-220° C., 2-chloromethyl-6-fluoroquinoline and m-resorcinol gave 3-(6-fluorocruinol-2-ylmethoxy)phenol, m.p. 146°-148° C. and 2-chloromethyl-5-fluorobenzothiazol and methyl 3-hydroxymandelate gave methyl 3-(5-fluorobenzothiazol-2-ylmethoxy)mandelate, m.p. 99°-101° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05322847
Quelldatensatzuspto-grants-1994_06
ORD IDord-6b4668dbade64491afd029d8e78a6fd4
Quellennotizuspto-grants-1994_06