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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8943Erstellt: 23. Oktober 2026

N-bromobutanimide → Ethyl 2-bromomethyl-6-methoxybenzoate

https://huagongshe.com/de/reaction/8943

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
Edukt2-Methoxy-6-methyl-benzoic acid ethyl esterHCID 591060—
KatalysatorBenzoyl PeroxideHCID 7187—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelCarbon TetrachlorideHCID 5943—
ProduktEthyl 2-bromomethyl-6-methoxybenzoateHCID 1003892660%

Reaktionsschritte

To a solution of ethyl 2-methoxy-6-methylbenzoate (0.813 g, 4.19 mmol) in CCl4 (8 mL) was added recrystallized N-bromosuccinimide (0.751 g, 4.22 mmol) followed by benzoyl peroxide (52 mg, 0.22 mmol). The resultant mixture was heated to reflux for 90 minutes then cooled to room temperature. The mixture was diluted with diethyl ether (50 mL), filtered through filter paper, and the filtrate was concentrated. Purification of the crude material by column chromatography (8:1 hexanes-EtOAc) provided 0.68 g (60%) of ethyl 6-(bromomethyl)-2-methoxybenzoate as a colorless oil. 1H NMR (CDCl3) δ 1.42 (t, 3H, J=7.2 Hz), 3.84 (s, 3H), 4.45 (q, 2H, J=7.2 Hz), 4.50 (s, 2H), 6.89 (d, 1H, J=8.4 Hz), 7.01 (d, 1H, J=7.2 Hz), 7.34 (dd, 1H, J=7.2, 8.4 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091217B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-f64e217233764463aa5656221e71fb06
Quellennotizuspto-grants-2006_08