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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 870037Erstellt: 23. Oktober 2026

Tributylphosphine → 5-chloro-3-(3-chlorobenzyl)-N-[1-(4-cyanophenyl)ethyl]thiophene-2-carboxamide

https://huagongshe.com/de/reaction/870037

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTributylphosphineHCID 13831—
EduktDiphenyl diselenideHCID 15460—
Edukt4'-CyanoacetophenoneHCID 74044—
EduktHCID 45140204HCID 45140204—
EduktHCID 57900982HCID 57900982—
LösungsmittelAcetonitrileHCID 6342—
Produkt5-chloro-3-(3-chlorobenzyl)-N-[1-(4-cyanophenyl)ethyl]thiophene-2-carboxamideHCID 57900981—

Reaktionsschritte

To a suspension of 5-chloro-3-(3-chlorobenzyl)thiopbene-2-carboxylic acid from Example 1, Step 6 (230 mg, 0.801 mmol), 4-(1-azidoethyl)benzonitrile (146 mg, 0.848 mmol) [prepared according to Thompson et al. J. Org. Chem. 1993, 58, 5886, after reduction of commercially available 4-acetylbenzonitrile] and diphenyl diselenide (549 mg, 1.76 mmol) in acetonitrile at r.t. under N2 was added tributylphosphine (217 μL, 0.881 mmol, 1.1 eq) dropwise (suspension dissolved, slightly exothermic) and the mixture was stirred at r.t. for 6 h, quenched with saturated NaHCO3 and extracted with ether. The crude was purified by Combi Flash chromatography system (10-40% EtOAc/hexane) to give the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08969394B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-27512fc6ee68476f8bc87d3b9152fbd4
Quellennotizuspto-grants-2015_03