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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490475Generated: October 25, 2026

Sodium Hydroxide → 5-Benzyl-3-hydroxyhexahydropyrrolo[3,4-c]pyrrol-1-one

https://huagongshe.com/reaction/490475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant5-Benzyl-octahydropyrrolo(3,4-c)pyrrole-1,3-dioneHCID 4564902—
ReactantAluminium lithium hydrideHCID 21226445—
Reactantrac-(3aR,6aS)-octahydropyrrolo[3,4-c]pyrrole-1,3-dioneHCID 51072220—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-Benzyl-3-hydroxyhexahydropyrrolo[3,4-c]pyrrol-1-oneHCID 6714761555%

Reaction Conditions

Temperature3 °C

Reaction Steps

A solution of 5-benzyltetrahydropyrrolo[3,4-c]pyrrole-1,3-dione, (12.7 g; 55 mmol) {preparation described for the preparation of cis-perhydropyrrolo[3,4-c]pyrrole-1,3-dione (b)} is added to a suspension of lithium aluminum tetrahydride (2 g; 55 mmol) in tetrahydrofuran, cooled to 3° C. in an ice bath, in a 500 ml three-necked flask. The reaction mixture is agitated at this temperature for 25 minutes and then water (2 ml), 4 N aqueous sodium hydroxide (2 ml) and water (6 ml) are successively added. The solid thus formed is removed by filtration; the filtrate is dried over magnesium sulfate and then evaporated under reduced pressure, resulting in a white solid which is triturated in diisopropyl ether (50 ml). The solid formed is filtered off, washed with diisopropyl ether (25 ml), and then dried under reduced pressure at constant weight. 5-Benzyl-3-hydroxyhexahydropyrrolo[3,4-c]pyrrol-1-one (7 g; 55%) is isolated, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528147B2
Source datasetuspto-grants-2009_05
ORD IDord-f23182a2566c4bac93666d927a3a49ff
Source noteuspto-grants-2009_05