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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238528Generated: October 26, 2026

Pivalaldehyde → 1-(2,2-Dimethylpropyl)-5-oxoproline

https://huagongshe.com/reaction/2238528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivalaldehydeHCID 12417—
ReactantSodium HydroxideHCID 14798—
ReactantL-Glutamic AcidHCID 33032—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Product1-(2,2-Dimethylpropyl)-5-oxoprolineHCID 6745917855.2%

Reaction Steps

L-glutamic acid (1.47 g, 10 mmol) was dissolved in 2N aqueous sodium hydroxide (10 ml, 20 mmol) and treated with a solution of trimethylacetaldehyde (1.09 ml, 10 mmol) in ethanol (5 ml) and then stirred at room temperature for 30 minutes. The mixture was cooled to 0° C. and treated with sodium borohydride (0.130 g). The mixture was allowed to warm to room temperature with stirring over 4 hrs and then acidified to neutral pH. Concentration in vacuo was followed by slurrying in ethanol and azeotroping three times with more ethanol. Finally the remaining material was suspended in ethanol (50 ml) and heated at reflux for 48 hrs. The mixture was then cooled to room temperature, salts were filtered off and the solvent was evaporated in vacuo to give a gum. Trituration with diethyl ether followed by drying afforded pure solid 1-(2,2-dimethylpropyl)-5-oxoproline (1.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718693B2
Source datasetuspto-grants-2010_05
ORD IDord-e9356e52b1de4022b43e38b33b87b288
Source noteuspto-grants-2010_05