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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601660Generated: October 26, 2026

Methanol → tert-Butyl 5-bromo-1-oxoisoindoline-2-carboxylate

https://huagongshe.com/reaction/601660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantCarbonic acid, bis(1,1-dimethylethyl) esterHCID 10219638—
Reactant5-bromo-2,3-dihydro-1H-isoindol-1-oneHCID 22607119—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 5-bromo-1-oxoisoindoline-2-carboxylateHCID 2315815449.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

Under nitrogen atmosphere, 70 mg of 5-bromo-1-oxo-isoindoline was dissolved in 2 ml of tetrahydrofuran, cooled down to 0° C., and then 4 mg of N,N-dimethylaminopyridine and 144 mg of di-tert-butylcarbonate were added. The mixture was stirred at room temperature for 30 min. Methanol was added to the reaction solution, and the solvents were distilled outunder reduced pressure. Water was added to the residues, extracted with ethyl acetate. Ethyl acetate layer was washed with saturated saline solution, and dried with anhydrous sodium sulfate. After distilling out the solvents under reduced pressure, the residues were separated and purified by silicagel column chromatography (ethyl acetate/hexane=1/2), to obtain 51.2 mg of the above compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902369B2
Source datasetuspto-grants-2011_03
ORD IDord-f97bee4de3f744e89a8f2519c789c528
Source noteuspto-grants-2011_03