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HRID 419682Erstellt: 25. Oktober 2026

Phthalic Anhydride → (2S)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionic acid tert-butyl ester

https://huagongshe.com/reaction/419682

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhthalic AnhydrideHCID 6811—
EduktDiisopropylethylamineHCID 81531—
Edukttert-Butyl alaninate hydrochlorideHCID 11275390—
LösungsmittelTolueneHCID 1140—
LösungsmittelDiethyl EtherHCID 3283—
Produkt(2S)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionic acid tert-butyl esterHCID 1300579790%

Reaktionsschritte

A suspension of (2S) alanine tert-butyl ester hydrochloride (2.05 g, 11.2 mmol), diisopropylethylamine (1.83 mL, 10.6 mmol) and phthalic anhydride (1.48 g, 10 mmol) in toluene (10 mL) was refluxed for 3 hours under Dean-Stark conditions. The reaction was cooled to room temperature, diluted with Et2O, washed with 1N HCl and then with aq.sat. NaHCO3. The organic layer was dried (MgSO4), filtered and evaporated to afford the sub-title compound as a white powder (2.465 g, 90%): 1H NMR (400 MHz CDCl3) δ 1.45 (9H, s), 1.68 (3H, d), 4.90 (1H, q), 7.75 (2H, d), 7.88 (2H, d).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093392B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-7080ca3fd18f490992ab57905ba4463c
Quellennotizuspto-grants-2012_01