Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1987573Erstellt: 25. Oktober 2026

Hydrochloric Acid → (2S)-2-(4-chloro-benzenesulfonylamino)-5,5,5-trifluoro-3-(2,2,2-trifluoroethyl)pentanoic acid methyl ester

https://huagongshe.com/reaction/1987573

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPyridineHCID 1049—
Edukt4-Chlorobenzenesulfonyl chlorideHCID 7398—
Edukt(2S)-2-amino-5,5,5-trifluoro-3-(2,2,2-trifluoroethyl)-pentanoic acid methyl esterHCID 25112112—
LösungsmittelDichloromethaneHCID 6344—
Produkt(2S)-2-(4-chloro-benzenesulfonylamino)-5,5,5-trifluoro-3-(2,2,2-trifluoroethyl)pentanoic acid methyl esterHCID 2511211384,4%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

To a solution of (2S)-2-amino-5,5,5-trifluoro-3-(2,2,2-trifluoroethyl)pentanoic acid methyl ester (2.173 g, 8.14 mmol) and pyridine (1.97 mL, 24.4 mmol) in CH2Cl2 (15 mL) was added a solution of 4-chlorobenzenesulfonyl chloride (2.66 g, 12.2 mmol, 97% pure) in CH2Cl2 (7 mL). The reaction mixture was stirred at 25° C. for 4 h, then cooled to 0° C. 15 mL of 1N HCl was added followed by 10 mL of dichloromethane. The phases were separated. The organic phase was washed with 1N HCl (15 mL) and brine, dried over Na2SO4, and concentrated to afford 4.1 g of crude mixture as a yellow solid. The solids were recrystallized from heptane (14 mL) to afford 3.035 g of the title product (84% yield). Mass Spectrum (+ESI): 442 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07550629B2
Quelldatensatzuspto-grants-2009_06
ORD IDord-a36093cf7f47453992a151119d72c4b1
Quellennotizuspto-grants-2009_06