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HRID 1741414Erstellt: 26. Oktober 2026

Triethylamine → 1-[4,5-Bis(4-methylphenyl)oxazol-2-yl)butan-1,4-dione

https://huagongshe.com/reaction/1741414

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-Pyridinesulfonic acidHCID 94849—
Edukt4-Hydroxy-1-(4,5-bis(4-methylphenyl)-oxazol-2-yl)butan-1-oneHCID 18367335—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt1-[4,5-Bis(4-methylphenyl)oxazol-2-yl)butan-1,4-dioneHCID 1836734728,4%

Reaktionsschritte

To a solution of 4-hydroxy-1-[4,5-bis(4-methylphenyl)oxazol-2-yl)butan-1-one (0.78 g) and triethylamine (2 ml) in DMSO (10 ml) was added a solution of pyridinesulfonic acid (1.16 g) in DMSO (4 ml) at room temperature. After being stirred for 20 minutes at the same temperature, the mixture was partitioned between ethyl acetate and water. The organic layer was washed with 1M-HCl, water and brine. The dried solvent was evaporated in vacuo and the residue was purified by chromatography on silica gel to give 1-[4,5-bis(4-methylphenyl)oxazol-2-yl)butan-1,4-dione (0.22 g). MS (m/z): 334 (M+ +1) IR (Nujol): 1735, 1690 cm-1NMR (CDCl3, δ): 2.38 (3H, s), 2.40 (3H, s), 2.97 (2H, t, J=6.4 Hz), 3.47 (2H, t, J=6.4 Hz), 7.17-7.26 (4H, m), 7.53-7.59 (4H, m), 9.88 (1H, s)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05972965
Quelldatensatzuspto-grants-1999_10
ORD IDord-ade7e75b1a8a4fae9720327ce81bd397
Quellennotizuspto-grants-1999_10