(5S)-5-(2-Methylpropyl)pyrrolidine-2,4-dione → HCID 11768826, compound

HRID 346304Notes

Reaction equation

HRID 346304 reaction equation
[CH3:1][CH:2]([CH3:11])[CH2:3][C@@H:4]1[NH:8][C:7](=[O:9])[CH2:6][C:5]1=[O:10].[H][H]>C(O)C.[Ni]>[OH:10][C@@H:5]1[C@H:4]([CH2:3][CH:2]([CH3:1])[CH3:11])[NH:8][C:7](=[O:9])[CH2:6]1

Participants

5

Procedure

A solution of 5 g of (S)-5-(2-methylpropyl)-2,4-pyrrolidinedione in 250 ml of ethanol is treated with 2 g of Raney nickel (washed to neutral) and exposed to hydrogen gas at 50 pounds per square inch (psi). After 5 hours, hydrogen uptake ceases, the catalyst is filtered and the filtrate evaporated to a gum. The gum is taken up in chloroform and the chloroform is evaporated. The resulting gum is dissolved in chloroform, filtered through a 250 ml bed of silica gel in chloroform and eluted with chloroform-methanol (96:4) to afford 3.2 g of (4S-cis)-4-hydroxy-5-(2-methylpropyl)-2-pyrrolidinone after crystallization from 12 ml of hot ethyl acetate, 120 ml isopropyl ether and gradual cooling to 10° C.; mp 71°-73° C. [α]D23 =-19° (C=0.7% chloroform).

Workup

  1. filtrationhydrogen uptake ceases, the catalyst is filtered
  2. customthe filtrate evaporated to a gum
  3. customthe chloroform is evaporated
  4. dissolutionThe resulting gum is dissolved in chloroform
  5. filtrationfiltered through a 250 ml bed of silica gel in chloroform
  6. washeluted with chloroform-methanol (96:4)

Sources & evidence

ORD record
ord-215ab9d58cd84c3a975e0192257f6ed8
Source dataset
uspto-grants-1991_10
Patent number
US05061808

Reaction notes

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