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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1919898Erstellt: 26. Oktober 2026

Methyl 4-(bromomethyl)benzoate → Methyl 4-{3-tert-butoxy-2-[(tert-butoxycarbonyl)amino]-3-oxopropyl}benzoate

https://huagongshe.com/reaction/1919898

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 4-(bromomethyl)benzoateHCID 256687—
EduktLithium HexamethyldisilazideHCID 2733832—
Edukttert-Butyl ((tert-butoxycarbonyl)amino)acetateHCID 4097102—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
ProduktMethyl 4-{3-tert-butoxy-2-[(tert-butoxycarbonyl)amino]-3-oxopropyl}benzoateHCID 57611911—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Tert-butyl[(tert-butoxycarbonyl)amino]acetate (1.01 g, 4.37 mmol) was dissolved in THF (10 mL) and cooled to −78° C. LiHMDS (6.5 mL, 1M solution in THF) was slowly added and allowed to stir for 30 minutes. Methyl 4-(bromomethyl)benzoate (1.98 g, 8.64 mmol) in THF (6 mL) was added to the mixture and allowed to stir overnight, slowly warming to room temperature. The reaction was diluted with ethyl acetate and quenched with saturated ammonium chloride. The aqueous layer was extracted three times with ethyl acetate. The combined organic layer was dried over sodium sulfate, filtered, and concentrated. The resulting residue was purified by column chromatography. MS: cal'd 379 (MH+), exp 402 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08168658B2
Quelldatensatzuspto-grants-2012_05
ORD IDord-fd8c5cc610c84a5b9d787fb783e8e6d1
Quellennotizuspto-grants-2012_05