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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774378Generated: October 31, 2026

Acetic Anhydride → 2-(4-Acetoxybenzyl)-3-ethylmaleic anhydride

https://huagongshe.com/reaction/1774378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant3-(4-t-Butyldimethylsilyloxybenzyl)-2-ethyl-2-hydroxysuccinic acidHCID 66648566—
SolventToluene ethylacetateHCID 21584019—
Product2-(4-Acetoxybenzyl)-3-ethylmaleic anhydrideHCID 5970655179%

Reaction Conditions

Temperature115 °C

Reaction Steps

To the crude 3-(4-t-butyldimethylsilyloxybenzyl)-2-ethyl-2-hydroxysuccinic acid thus obtained was added acetic anhydride (5 mL), and the mixture was stirred at 115° C. for 3 h. The acetic anhydride was evaporated under reduced pressure, and the residue thus obtained was subjected to silica gel column chromatography (toluene-ethyl acetate 19:1→16:1) to give the title compound as oil in an amount of 210 mg (2 step yield: 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260375B2
Source datasetuspto-grants-2016_02
ORD IDord-6027c8cefc4a4ed8a77d32a47355d587
Source noteuspto-grants-2016_02