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HRID 555131Erstellt: 25. Oktober 2026

2,4-Dimethoxybenzoic acid → 5-Bromo-2,4-dimethoxybenzoic acid

https://huagongshe.com/reaction/555131

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4-Dimethoxybenzoic acidHCID 7052—
EduktBromineHCID 24408—
LösungsmittelChloroformHCID 6212—
Produkt5-Bromo-2,4-dimethoxybenzoic acidHCID 1350509778,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a 250 mL round-bottomed flask was added chloroform (60 mL) along with 2,4-dimethoxybenzoic acid (2.0 g, 10.98 mmol). The solution was cooled to 0° C. and bromine (0.566 mL, 10.98 mmol) was added dropwise over 5 minutes. The solution was allowed to warm to room temperature and stirred overnight. The resulting solid was filtered, washed with cold chloroform and dried under vacuum to give 2.49 g (8.6 mmol, 78% yield) of 5-bromo-2,4-dimethoxybenzoic acid as a yellow solid. The LC/MS data was obtained on a Shimadzu analytical LC/MICROMASS® Platform LC (ESI+) at 220 nm using the following set of conditions: PHENOMENEX® Luna 3 μm C18, 2×30 mm column, with a gradient of 0-100% B (B=90% HPLC grade acetonitrile/0.1% trifluoroacetic acid/10% HPLC grade water), (A=90% HPLC grade water/0.1% trifluoroacetic acid/10% HPLC grade acetonitrile), in 2 minutes with a 1 minute hold at a rate of 1.0 mL/minute. 1H NMR (400 MHz, DMSO-d6) δ ppm 3.88 (s, 3H), 3.95 (s, 3H), 6.78 (s, 1H), 7.86 (s, 1H). LCMS Rt=1.453 min., m/z 262.99 (M+H), 93% purity.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08048887B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-e9e117610ed848909f94ed936d3ad571
Quellennotizuspto-grants-2011_11