Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 532203Erstellt: 25. Oktober 2026

Sodium Bromide → 4-Bromo-3-iodotoluene

https://huagongshe.com/reaction/532203

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium BromideHCID 253881—
Edukt2-Iodo-4-methylanilineHCID 2764000—
EduktSodium NitriteHCID 23668193—
KatalysatorCopper SulfateHCID 24462—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelSulfuric AcidHCID 1118—
Produkt4-Bromo-3-iodotolueneHCID 1621808868%

Reaktionsschritte

To a mixture of 2-iodo-4-methylaniline (50 g, 214.55 mmol) in HOAc (250 mL), H2SO4 (10 mL), and H2O (40 mL) was added a solution of NaNO2 (14.5 g) in H2O (80 mL) at 0° C. The solution was stirred for 1.5 h. This was defined as mixture A. In another round bottom flask, a mixture of NaBr (107 g), CuSO4 (32.2 g), Cu (38.9 g), H2SO4 (39 mL), and H2O (25 mL) was refluxed for 1.5 h. To this mixture was added mixture A, and the solution was then refluxed for 3 h. The solution was treated with water and extracted with EA (500 mL×3). The combined organic layers were washed with brine, dried over Na2SO4, and then concentrated in vacuo. Purification by column chromatography over silica gel eluted with PE afforded the product as colorless oil (43 g, yield 68%). 1H NMR (300 MHz, CDCl3): δ 7.69 (m, 1H), 7.47 (d, J=8.1 Hz, 1H), 7.00 (m, 1H), 2.26 (s, 3H) ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08853186B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-e2e8792fee26474b83fb3560bfdcff3a
Quellennotizuspto-grants-2014_10