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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1672611Erstellt: 27. Oktober 2026

Trifluoroacetic acid → Methyl 4-({2-[2-(4-bromobenzyloxy)phenyl]ethylamino}methyl)benzoate

https://huagongshe.com/reaction/1672611

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktSodium BicarbonateHCID 516892—
EduktMethyl 4-[({2-[2-(4-bromobenzyloxy)phenyl]ethyl}-tert-butoxycarbonylamino)methyl]benzoateHCID 57864402—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 4-({2-[2-(4-bromobenzyloxy)phenyl]ethylamino}methyl)benzoateHCID 2201499593%

Reaktionsschritte

A solution of 4.2 g (7.57 mmol) of methyl 4-[({2-[2-(4-bromobenzyloxy)phenyl]ethyl}-tert-butoxycarbonylamino)methyl]benzoate from Example 4A in 15 ml of dichloromethane is stirred with 15 ml of trifluoroacetic acid at room temperature for 4 hours. The reaction solution is then neutralized with aqueous sodium bicarbonate solution, and the organic phase is separated off and dried over sodium sulfate. Filtration is followed by removal of the solvent in vacuo. 3.2 g (7.04 mmol, 92% yield) of a colorless oil are obtained which are employed in the next stage without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07998988B2
Quelldatensatzuspto-grants-2011_08
ORD IDord-ce317b1ed501428c99a18934d614935e
Quellennotizuspto-grants-2011_08