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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110812Generated: November 2, 2026

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

https://huagongshe.com/reaction/2110812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl alaninate hydrochlorideHCID 11275390—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product(2S)-2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propionic acid tert-butyl esterHCID 1300579790%

Reaction Steps

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)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517987B2
Source datasetuspto-grants-2009_04
ORD IDord-fbf1b0d61f6244fc8ca95ce1bc39d8c7
Source noteuspto-grants-2009_04