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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1582310Erstellt: 27. Oktober 2026

Diisobutylaluminum hydride → (4-(Benzo[d]thiazol-2-yl)phenyl)methanol

https://huagongshe.com/reaction/1582310

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisobutylaluminum hydrideHCID 14487—
Edukt4-Benzothiazol-2-yl-benzoic acid methyl esterHCID 7174175—
EduktPotassium sodium tartarateHCID 9855836—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(4-(Benzo[d]thiazol-2-yl)phenyl)methanolHCID 1704705475%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a 0° C. solution of methyl-4-(benzothiazol-2-yl)-benzoate (prepared as described by A. Brembilla, D. Roizard and P. Lochon Synth. Commun. 1990, 20, 3379) (1.08 g, 4 mmol) in THF (20 mL) was added DIBAL-H (20 mL of a 1.0 M solution in THF, 20 mmol) over 10 minutes. The resulting solution was stirred at 0° C. for 2 hours, then an aqueous saturated solution of sodium potassium tartrate was added and the biphasic mixture stirred rapidly for 60 min. The phases were separated and the aqueous layer extracted with ether (3×20 mL). The combined organic fractions were dried (Na2SO4), concentrated and purified by column chromatography on silica gel (10:1 CH2Cl2/MeOH) to afford the title compound (0.69 g, 75%). 1H NMR (CD3OD) δ4.69 (s, 2H), 7.43 (t, 1H, J=7.8 Hz), 7.53 (m, 3H), 7.99 (m, 1H), 8.06 (m, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06734191B2
Quelldatensatzuspto-grants-2004_05
ORD IDord-72e06e19a034437a9d7b884feff325bc
Quellennotizuspto-grants-2004_05