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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 36645Erstellt: 25. Oktober 2026

Sulfuric Acid → (S)-3-amino-2-benzenesulfonylamino-propionic acid tert-butyl ester hydrochloride

https://huagongshe.com/reaction/36645

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktIsobutyleneHCID 8255—
Edukt(2S)-3-amino-2-(benzenesulfonamido)propanoic AcidHCID 10752796—
EduktEther hydrochlorideHCID 10953452—
LösungsmittelChloroformHCID 6212—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt(S)-3-amino-2-benzenesulfonylamino-propionic acid tert-butyl ester hydrochlorideHCID 22853534—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

In a Fischer-Porter tube, a mixture of 22-2 (102 g, 42 mmol) and DME (150 mL) was sequentially treated with H2SO4 (6.4 mL, 0.12 mol), cooled to -78° C., and then condensed isobutylene (75 mL). The cooling bath removed. After 2 h, ice-water (250 mL) was added followed by washing with ether (2×). The aqueous phase was basified with aq 5N NaOH, then saturated with NaCl, followed by extraction with EtOAc (3×). The combined extracts were washed with brine dried (MgSO4), and concentrated to give a white solid. This was dissolved in CHCl3 then treated with 1N HCl/ether (22 mL) then concentrated to give 22-3 as a glossy yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05416099
Quelldatensatzuspto-grants-1995_05
ORD IDord-b0d0a3512ec748a0a355906b81a46fe3
Quellennotizuspto-grants-1995_05