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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2262864Erstellt: 26. Oktober 2026

Nitric Acid → 4,5-Dimethoxy-2-nitrophenol

https://huagongshe.com/reaction/2262864

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitric AcidHCID 944—
Edukt3,4-DimethoxyphenolHCID 16251—
LösungsmittelAcetic AcidHCID 176—
Produkt4,5-Dimethoxy-2-nitrophenolHCID 297121—

Reaktionsschritte

In SCHEME 9 3,4-dimethoxyphenol (36) is selectively nitrated with 70% HNO3 in AcOH to give 4,5-dimethoxy-2-nitrophenol (37) which is further converted to the corresponding triflate (38) with trifluoromethylsulfonic anhydride (Tf2O) and pyridine in dichloromethane. Triflate (38) is reacted under inert conditions with a boronic acid of general type (31) under Suzuki-type basic conditions (Pd(PPh3)4 and aqueous potassium phosphate in toluene) to a biaryl of type (39). Biaryl (39) is further hydrolized with aqueous lithium hydroxide in THF and MeOH or MeCN to give the corresponding carboxylic acid (40) which is converted to a building block of type (41) by reaction with oxalyl chloride in anhydrous dichloromethane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07851501B2
Quelldatensatzuspto-grants-2010_12
ORD IDord-470721f2c58e44d09b9fdde48812aa67
Quellennotizuspto-grants-2010_12