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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1579051Erstellt: 27. Oktober 2026

Tert-Butylamine → Propan-2-ol, 1-tert-butylamino-3-[4-(1,2,3-thiadiazol-4-yl)phenoxy]-

https://huagongshe.com/reaction/1579051

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTert-ButylamineHCID 6385—
Edukt4-[4-(Oxiran-2-ylmethoxy)phenyl]-1,2,3-thiadiazoleHCID 2737103—
Lösungsmitteltert-ButanolHCID 6386—
ProduktPropan-2-ol, 1-tert-butylamino-3-[4-(1,2,3-thiadiazol-4-yl)phenoxy]-HCID 559440—

Reaktionsschritte

To a solution of 660 mg. of 4-[4(2,3-epoxypropoxy)phenyl]-1,2,3-thiadiazole in 29.7 ml. of t-butylamine is added 3.3 ml. of t-butanol and the reaction mixture is stirred at room temperature for 24 hours. It is then evaporated to dryness under vacuo and the residue taken up in methylene chloride. The resulting solution is extracted with dilute hydrochloric acid and the aqueous phase made alkaline with sodium carbonate. It is then extracted with ethyl acetate and the organic extracts washed to neutrality, dried over sodium sulfate and evaporated to dryness. The solid residue is purified by two recrystallizations from methylene chloridehexane (after decolorization with charcoal) and then by three crystallizations from benzene, thus obtaining the pure 4-[4(3-t-butylamino-2-hydroxypropoxy)phenyl]-1,2,3-thiadiazole, m.p. 124°-125° C; λmax 256, 304 nm, (ε 20,000;2,000) ir 3340, 1615, 1580, 1535, 835 cm-1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03940407
Quelldatensatzuspto-grants-1976_02
ORD IDord-f3c988459c774184a59f24eef17ca18e
Quellennotizuspto-grants-1976_02