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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 916498Erstellt: 25. Oktober 2026

Hydrochloric Acid → 4-[4-(Benzenesulfonylamino)-phenyl]-butyric acid

https://huagongshe.com/reaction/916498

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktLithium HydroxideHCID 3939—
EduktBenzenesulfonyl chlorideHCID 7369—
EduktTriethylamineHCID 8471—
EduktAmmonium ChlorideHCID 25517—
EduktMethyl 4-aminobenzenebutanoateHCID 88628—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-[4-(Benzenesulfonylamino)-phenyl]-butyric acidHCID 984003596,7%

Reaktionsschritte

To a solution of 40 (500 mg, 2.59 mmol) in CH2Cl2 at room temperature were added Et3N (901 μL, 6.48 mmol) followed by benzenesulfonyl chloride (661 μL, 5.18 mmol). The mixture was stirred overnight at room temperature then treated with a saturated aqueous solution of NH4Cl. The phases were separated and the organic layer was extracted several times with CH2Cl2. The combined organic extracts were dried over (MgSO4) then evaporated under reduced pressure. The residue was dissolved in a solvent mixture of THF (25 mL) and water (25 mL) then LiOH (1.08 g, 25.9 mmol) was added. The mixture was heated at 50° C. for 1 h then treated with HCl (1N) until pH2. The phases were separated and the aqueous layer was extracted several times with AcOEt. The combined organic extracts were dried over (MgSO4) then evaporated. The crude was purified by flash chromatography using CH2Cl2/MeOH (95:5) as solvent mixture yielding 41 (800 mg, 96%) as a white solid

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE039850E1
Quelldatensatzuspto-grants-2007_09
ORD IDord-cb0847c1f65f43d4a9e1ee3acae7bff8
Quellennotizuspto-grants-2007_09