Hydrogen Peroxide → (R)-2,5dihydro-pyrrole-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester

HRID 1385794Notes

Reaction equation

HRID 1385794 reaction equation
[CH3:1][CH2:2][O:3][C:4]([C@H:6]1[CH2:10][C@H:9]([Se]C2C=CC=CC=2)[CH2:8][N:7]1[C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])=[O:5].N1C=CC=CC=1.OO>ClCCl>[CH3:1][CH2:2][O:3][C:4]([C@H:6]1[CH:10]=[CH:9][CH2:8][N:7]1[C:18]([O:20][C:21]([CH3:22])([CH3:24])[CH3:23])=[O:19])=[O:5]

Participants

5

Reactant 3

HCID 784Hydrogen PeroxideHCID 1049PyridineHCID 57984825(2R,4S)-4-Phenylselanyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester

Product 1

HCID 53653320(R)-2,5dihydro-pyrrole-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl esterYield 77.5%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of 7.35 g (0.016 mol) (2R,4S)-4-phenylselanyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester in 80 ml dichloromethane were added at 0-5° C. 1.93 ml (0.024 mol) pyridine and 4.6 ml 30% hydrogen peroxide and stirring was continued for 1.5 hours. The mixture was extracted with 5% aqueous HCI, saturated aqueous sodium carbonate, and water. Chromatography on silicagel with ethylacetatelhexane 1:5 yielded 2.99 g (77%) (R)-2,5dihydro-pyrrole-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester as colorless oil. MS m/e (%): 186 (11), 168 (48), 140 (32), 112(100), 68 (85), 57 (58). [α]D=+242° (c=1% in chloroform).

Workup

  1. extractionThe mixture was extracted with 5% aqueous HCI, saturated aqueous sodium carbonate, and water

Sources & evidence

ORD record
ord-03c5bb02b50f4dd29ec1ea7a39833c4a
Source dataset
uspto-grants-2001_07
Patent number
US06262089B1

Reaction notes

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