Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1811723Erstellt: 27. Oktober 2026

Acetic Acid → Methyl 2,4-dichloro-5-iodobenzoate

https://huagongshe.com/reaction/1811723

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktTrimethylsilyldiazomethaneHCID 167693—
Edukt2,4-Dichloro-5-iodobenzoic acidHCID 68417909—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 2,4-dichloro-5-iodobenzoateHCID 57898875—

Reaktionsschritte

Sodium iodate (4.4 g) and iodine (11.1 g) were added to 90% sulfuric acid (330 ml) and stirred at room temperature for 8 hours. Commercially available 2,4-dichlorobenzoic acid (21 g) was added and stirred at the same temperature for 24 hours. The reaction solution was poured onto ice water (3 l), and the precipitated solid material was separated by filtration. The solid material was then washed with water, and dried under reduced pressure. 2,4-Dichloro-5-iodobenzoic acid (16.8 g) was obtained by recrystallization (acetic acid-water). 2,4-Dichloro-5-iodobenzoic acid (2 g) was dissolved in dichloromethane (20 ml) and methanol (20 ml), and trimethylsilyldiazomethane (2 M; n-hexane solution) was added dropwise thereto until the solution became yellow. After a small amount of acetic acid was added, the mixture was concentrated under reduced pressure. The resulting residue was recrystallized from n-hexane to yield the title compound 2,4-dichloro-5-iodobenzoic acid methyl ester (2 g) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08362236B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-cb81da8f88dc4391bfd44178b19d0a4c
Quellennotizuspto-grants-2013_01