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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743901Generated: October 26, 2026

(S)-N-Benzylglutamic acid → (S)-1-Benzyl-5-carboxy-2-pyrrolidinone

https://huagongshe.com/reaction/743901

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-N-Benzylglutamic acidHCID 11107380—
SolventWaterHCID 962—
Product(S)-1-Benzyl-5-carboxy-2-pyrrolidinoneHCID 1090011398.9%

Reaction Steps

N-Benzyl-glutamic acid (35 g) was dissolved in 300 ml of water and refluxed for 15 hours. The solution was extracted with methylene chloride, washed with brine, dried over sodium sulfate and concentrated to yield 32 g of N-benzyl-5-oxo-proline. The acid (55.25 mmoles, 12.1 g) was dissolved in 15 ml of DMF and 30 ml acetonitrile. The solution was cooled to -25° C. Oxalyl chloride (5.0 ml) in 10 ml acetonitrile was added. The solution was stirred vigorously for 30 minutes. A solution of t-butanol (135 mmoles, 10.0 g) and pyridine (13.2 g) in 10 ml acetonitrile was added over 30 minutes and then warmed to 0° C. Brine and ethyl acetate were added. The organic phase was diluted and washed with water, dried and concentrated to yield 10.7 g of N-benzyl-5-oxo-L-proline t-butyl ester. (MS)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556981
Source datasetuspto-grants-1996_09
ORD IDord-524e94e891e14a8c892d4aa4b0237283
Source noteuspto-grants-1996_09