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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1170255Erstellt: 27. Oktober 2026

Dicyclohexylcarbodiimide → Methyl 4-(bromomethyl)-3-nitrobenzoate

https://huagongshe.com/reaction/1170255

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt4-Bromomethyl-3-nitrobenzoic acidHCID 132386—
Edukt4-pyridinemethanamine, N,N-dimethyl-HCID 264946—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelDichloromethane methanolHCID 21226129—
ProduktMethyl 4-(bromomethyl)-3-nitrobenzoateHCID 13399987—

Reaktionsschritte

A solution of dicyclohexylcarbodiimide (DCC, 0.95 g, 4.61 mmol, 1.2 equiv) in 10 mL of dichloromethane (DCM) was added dropwise to a stirred mixture of 4-bromomethyl-3-nitro-benzoic acid 1 (1.0 g, 3.84 mmol, 1.0 equiv) and 4-dimethylaminomethylpyridine (DMAP) (0.020 g, 0.19 mmol, 0.05 equiv) in 10 mL of dichloromethane-methanol (10%) at room temperature. The mixture was stirred for 6 hours to obtain 4-bromomethyl-3-nitro-benzoic acid methyl ester 2. Dicyclohexyl urea (DCU) thus obtained was removed by filtration and the solvent in the filtered solution was removed under vacuum. The residue was purified by column chromatography using hexane-ethyl acetate (15%) as an eluant to give ester 2 as a light yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07825261B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-b2ed8b5eb7294125b0663e5aa2c912fc
Quellennotizuspto-grants-2010_11