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HRID 64126Erstellt: 24. Oktober 2026

Nitrogen → N-(2',5'-difluoro-5-nitrobiphenyl-3-yl)acetamide

https://huagongshe.com/de/reaction/64126

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
EduktSodium CarbonateHCID 10340—
Edukt(2,5-Difluorophenyl)boronic acidHCID 2734335—
EduktN-(3-bromo-5-nitrophenyl)acetamideHCID 10658908—
KatalysatorBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
ProduktN-(2',5'-difluoro-5-nitrobiphenyl-3-yl)acetamideHCID 11777762767%

Reaktionsschritte

A solution of N-(3-bromo-5-nitrophenyl)acetamide of Example 1(c) (0.8 g, 3.07 mmol) in 1,2-dimethoxyethane (15 ml) was degassed by N2 bubbling for 5 min. 2,5-Difluorophenylboronic acid (0.58 g, 3.69 mmol, 1.2 eq.) was added and the mixture was degassed for another 5 min. Pd(dppf)Cl2 (0.5 g, 0.615 mmol, 0.2 eq.) and aqueous sodium carbonate (0.98 g, 9.23 mmol, 3.0 eq.) were added and the procedure of Example 1(d) was followed. The crude residue of the product was purified by column chromatography (60-120 silica gel, 25% ethyl acetate in hexane) to give the product in 67% yield (0.6 g). 1H NMR (300 MHz, DMSO-d6): δ 10.56 (s, 1H), 8.65 (t, 1H), 8.14 (s, 1H), 8.06 (s, 1H), 7.56-7.52 (m, 1H), 7.47-7.37 (m, 2H), 2.12 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447091B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-212d617d48bb4a4989bcc60b5c002bb1
Quellennotizuspto-grants-2016_09