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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078477Generated: October 31, 2026

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

https://huagongshe.com/reaction/2078477

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 numberUS07928246B2
Source datasetuspto-grants-2011_04
ORD IDord-2002ce54c94c49beadc8e16fb0c22bd6
Source noteuspto-grants-2011_04