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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492236Generated: October 30, 2026

Bromoacetic Acid → (2-Benzyl-3-oxo-2,3-dihydro-1H-isoindol-1-yloxy)-acetic acid

https://huagongshe.com/reaction/492236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetic AcidHCID 6227—
ReactantSodium hydrideHCID 24758—
Reactant2-benzyl-3-hydroxy-2,3-dihydro-1H-isoindol-1-oneHCID 3240743—
SolventTetrahydrofuranHCID 8028—
Product(2-Benzyl-3-oxo-2,3-dihydro-1H-isoindol-1-yloxy)-acetic acidHCID 1061392640.2%

Reaction Steps

To a suspension of sodium hydride (1.1 g, 38.5 mmol) in THF (30 mL) at room temperature was added a solution of compound 20 (2.0 g, 8.37 mmol) in THF (15 mL) and the resulting reaction mixture was allowed to stir at room temperature for 1 hour. Thereafter a solution of bromo acetic acid (2.68 g, 19.25 mmol) in THF (5 mL) was added dropwise and the resulting reaction mixture was allowed to stir at room temperature for 18 hours. The reaction mixture is poured onto water and extracted with ethyl ether (3×100 mL) and the combined ethyl ether extracts were dried over anhydrous sodium sulfate and concentrated in vacuo. Chromatography (SiO2, 20 to 70% EtOAc-Hexanes eluant) provided 1.0 g of 22 as a clear oil (2.48 g, theoretical, 40% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531671B2
Source datasetuspto-grants-2009_05
ORD IDord-5eea9b605c91468b82e43765d99e2958
Source noteuspto-grants-2009_05