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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 63233Erstellt: 24. Oktober 2026

Pentane → (2-(4-Chlorophenyl)-1-(phenylsulfonyl)-1H-imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanone

https://huagongshe.com/de/reaction/63233

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPentaneHCID 8003—
EduktBenzoyl chloride, 3,4,5-trimethoxy-HCID 78282—
Edukt2-(4-Chlorophenyl)-1-(phenylsulfonyl)-1H-imidazoleHCID 49788500—
EduktHCID 178418306HCID 178418306—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelSodium BicarbonateHCID 516892—
Produkt(2-(4-Chlorophenyl)-1-(phenylsulfonyl)-1H-imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanoneHCID 4978880236,8%

Reaktionsschritte

To a solution of 2-(4-chlorophenyl)-1-(phenylsulfonyl)-1H-imidazole (10f) (6.0 mmol) in anhydrous THF (30 mL) at −78° C. was added 1.7 M tert-butyllithium in pentane (5.3 mL, 9.0 mmol) and stirred for 10 min. 3,4,5-Trimethoxybenzoyl chloride (7.2 mmol) was added at −78° C. and stirred for overnight. The reaction mixture was diluted with 100 mL of saturated NaHCO3 solution (aqueous) and extracted by ethyl acetate (200 mL). The organic layer was dried over magnesium sulfate and concentrated. The residue was purified by flash column chromatography (hexane:ethyl acetate 4:1) to give a white solid. Yield: 36.8%; 1H NMR (500 MHz, CDCl3) δ 8.05 (d, J=7.5 Hz, 2H), 7.77 (t, J=7.5 Hz, 1H), 7.62 (t, J=8.0 Hz, 2H), 7.48 (s, 1H), 7.44 (d, J=9.0 Hz, 2H), 7.39 (d, J=8.5 Hz, 2H), 7.37 (s, 2H). MS (ESI): calculated for C25H21ClN2O6S, 512.1. found 513.1 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447049B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-e16d5251861942d0865ec6ca7d3f8d39
Quellennotizuspto-grants-2016_09