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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 913807Erstellt: 26. Oktober 2026

Potassium Bromide → 2-Bromo-6-methyl-4-(trifluoromethyl)aniline

https://huagongshe.com/reaction/913807

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium BromideHCID 253877—
EduktSodium BicarbonateHCID 516892—
Edukt4-Amino-3-methylbenzotrifluorideHCID 13750437—
EduktSodium;3-oxidodioxaborirane;tetrahydrateHCID 23693097—
KatalysatorAmmonium paramolybdate tetrahydrateHCID 16211167—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
Produkt2-Bromo-6-methyl-4-(trifluoromethyl)anilineHCID 53416679—

Reaktionsschritte

To a suspension of 2-methyl-4-(trifluoromethyl)aniline (7.78 g, 44.4 mmol), potassium bromide (1.59 g, 13.3 mmol), and ammonium heptamolybdate tetrahydrate (140 mg, 0.111 mmol) in acetic acid (40 mL) at room temperature (in a room temperature waterbath) was added sodium perborate tetrahydrate (1.88 g, 12.2 mmol). After 10 min, the reaction was treated with an additional portion of potassium bromide (1.59 g, 13.3 mmol), ammonium heptamolybdate tetrahydrate (140 mg, 0.111 mmol), and sodium perborate tetrahydrate (1.88 g, 12.2 mmol). After 10 min, the reaction was treated with an additional portion of potassium bromide (1.59 g, 13.3 mmol), ammonium heptamolybdate tetrahydrate (140 mg, 0.111 mmol), and sodium perborate tetrahydrate (1.88 g, 12.2 mmol). After 10 min, the reaction was treated with an additional portion of potassium bromide (1.59 g, 13.33 mmol), ammonium heptamolybdate tetrahydrate (140 mg, 0.111 mmol), and sodium perborate tetrahydrate (1.88 g, 12.2 mmol). After 1 h, the reaction was treated with a final portion of everything in half the amounts of the previous additions. After 1 h, the mixture was poured into water, neutralized with solid sodium bicarbonate, extracted into diethyl ether, washed with water, then brine, dried over magnesium sulfate, and concentrated to give 11.3 g (100%) as an oil. 1H-NMR (CDCl3, 500 MHz) δ 7.56 (s, 1H), 7.23 (s, 1H), 4.36 (bs, 2H), 2.23 (s, 3H); 13C-NMR (CDCl3, 126 MHz) δ 145.3, 127.7 (q, J=3.8 Hz), 126.4 (q, J=3.8 Hz), 124.0 (q, J=272 Hz), 120.6 (q, J=34 Hz), 108.2, 18.3. Mass spec.: 253.95 (MH)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08026257B2
Quelldatensatzuspto-grants-2011_09
ORD IDord-2d55ca11fb7f49f89ff170d3ce86f66e
Quellennotizuspto-grants-2011_09