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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37832Erstellt: 24. Oktober 2026

Benzyl Bromide → 2-(Benzyloxy)-1-chloro-4-nitrobenzene

https://huagongshe.com/de/reaction/37832

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktPotassium CarbonateHCID 11430—
Edukt2-Chloro-5-nitrophenolHCID 69264—
LösungsmittelAcetoneHCID 180—
Produkt2-(Benzyloxy)-1-chloro-4-nitrobenzeneHCID 1288193399%

Reaktionsschritte

Benzyl bromide (0.6 mL, 5.04 mmol) was added dropwise to a mixture of 2-chloro-5-nitro-phenol (800 mg, 4.61 mmol) and potassium carbonate (1.27 g, 9.22 mmol) in acetone (20 mL) at room temperature and heated at reflux for 2 h. Inorganic salts were filtered off and washed with acetone (20 mL). The combined filtrate and washings were concentrated in vacuo, the resulting residue then being dissolved in ethyl acetate (25 mL) and washed successively with water (2×20 mL), brine (20 mL), dried over anhydrous sodium sulfate and concentrated in vacuo to yield 2-benzyloxy-1-chloro-4-nitro-benzene (1.20 g, 99%) as a cream solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524705B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-c6b6cd300ebe4d5bb2b195e5a8862289
Quellennotizuspto-grants-2013_09