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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1509888Erstellt: 27. Oktober 2026

1-Methylimidazole → (2-amino-5-chlorophenyl)(1-methyl-1H-imidazol-2-yl)methanone

https://huagongshe.com/reaction/1509888

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-MethylimidazoleHCID 1390—
Edukt2-Amino-5-chlorobenzoic acidHCID 12476—
EduktAmmonium ChlorideHCID 25517—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelHexaneHCID 8058—
Produkt(2-amino-5-chlorophenyl)(1-methyl-1H-imidazol-2-yl)methanoneHCID 1099897713,7%

Reaktionsschritte

To a solution of nBuLi (0.0730 mol) in hexane was added N-methyl imidazole (0.0608 mol) drop wise at −40° C. over 30 min under a nitrogen atmosphere. The resulting yellow solution was stirred for a further 3 hr at rt, and then refluxed for 1 h. 2-amino-5-chlorobenzoic acid (1.74 g, 0.01014 mole) in dry ether (60 ml) was then added to the reaction mixture. The reaction mixture was stirred overnight at rt. To the reaction mixture was added saturated NH4Cl solution and the resulting mixture extracted with ethyl acetate (2×150 ml). The combined organic layers were dried over Na2SO4. After removal of solvent, the residue was purified by the flash chromatography using ethyl acetate/hexane (1:4) as eluent. Crystallization of the product from Et2O/hexane mixture gave 300 mg (13.7%) of product as yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08211896B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-1e3543d5702f4f0db3b630f63bb99fcc
Quellennotizuspto-grants-2012_07