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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1068579Erstellt: 26. Oktober 2026

Hydrochloric Acid → 3,4-Dimethoxyphenyl 2-thiazolyl ketone

https://huagongshe.com/reaction/1068579

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt3,4-DimethoxybenzonitrileHCID 74842—
Edukt2-BromothiazoleHCID 76430—
EduktSodium BicarbonateHCID 516892—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelHexaneHCID 8058—
Produkt3,4-Dimethoxyphenyl 2-thiazolyl ketoneHCID 2118976846,5%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A hexane solution of butyllithium (9.50 mM) was dissolved in dried diethyl ether (6.5 ml) and cooled to −78° C. A solution of 2-bromothiazole (1.03 g, 6.13 mM) in diethyl ether (0.5 ml) was dropped into this solution. The solution was stirred at that temperature for 30 minutes, then a solution of 3,4-dimethoxybenzonitrile (1.00 g, 6.13 mM) in diethyl ether (3.0 ml) was added and the resultant mixture stirred for a further 6 hours. 1N Hydrochloric acid (20 ml) was poured into the solution obtained, which was then warmed to room temperature and stirred for 30 minutes, then a saturated sodium hydrogencarbonate solution was added to neutralize the solution and extraction was performed with ethyl acetate. Next, the organic layer was washed with brine and dried over anhydrous magnesium sulfate, then the solvent was removed in vacuo to obtain a dark red solid residue. The residue was purified by flash chromatography (SiO2: eluted by gradient from 50% hexane/methylene chloride to 25% hexane/methylene chloride). The solvent was removed in vacuo and the resultant product was dried to obtain 3,4-dimethoxyphenyl 2-thiazolyl ketone 0.71 g (yield 46.5%) as a red solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06251897B1
Quelldatensatzuspto-grants-2001_06
ORD IDord-39e331ceaef847f59d5e01b8cee33013
Quellennotizuspto-grants-2001_06