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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 264312Erstellt: 26. Oktober 2026

Ethyl bromoacetate → Ethyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]acetate

https://huagongshe.com/reaction/264312

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl bromoacetateHCID 7748—
EduktSodium hydrideHCID 24758—
EduktN-benzyl-4-methoxybenzenesulfonamideHCID 741351—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]acetateHCID 3503631—

Reaktionsschritte

Sodium hydride (1.56 g of a 50% oil dispersion, 33.0 mmol) is suspended in tetrahydrofuran (85 mL). To this is added a solution of N-[4-methoxybenzenesulfonyl]-benzylamine (9.0 g, 32.5 mmol) also in tetrahydrofuran (85 mL), and the reaction is stirred for 30 minutes at room temperature. Then ethyl bromoacetate (5.40 mL, 48.8 mmol) is added, and the reaction is stirred overnight at room temperature. The reaction is quenched with a small amount of water, and all the solvent is removed. The crude mixture is partitioned between ethyl acetate and water, the aqueous phase is extracted several times with ethyl acetate, the combined organic layers are dried (Na2SO4), and the solvent is evaporated. The product is purified by silica gel chromatography (30% ethyl acetate/hexane) to give ethyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]acetate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05646167
Quelldatensatzuspto-grants-1997_07
ORD IDord-69b12a99fb6745e3a0dca42796a9ff98
Quellennotizuspto-grants-1997_07