Hydrochloric Acid → 1-(4-Oxocyclohexyl)pyrrolidin-2-one

HRID 2175540Notes

Reaction equation

HRID 2175540 reaction equation
O1[C:5]2([CH2:10][CH2:9][CH:8]([N:11]3[CH2:15][CH2:14][CH2:13][C:12]3=[O:16])[CH2:7][CH2:6]2)[O:4]CC1.Cl>C(#N)C>[O:4]=[C:5]1[CH2:6][CH2:7][CH:8]([N:11]2[CH2:15][CH2:14][CH2:13][C:12]2=[O:16])[CH2:9][CH2:10]1

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 109002931-(1,4-Dioxaspiro[4.5]decan-8-yl)pyrrolidin-2-one

Product 1

HCID 585626831-(4-Oxocyclohexyl)pyrrolidin-2-oneYield 99.1%

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

1-(1,4-dioxaspiro[4.5]decan-8-yl)pyrrolidin-2-one (143 mg, 0.64 mmol) from above step B, was dissolved in acetonitrile, treated with 6N HCl, and stirred at room temperature for 18 h. reaction mixture was concentrated in vacuo, treated with saturated NaHCO3 to pH 6. The solvents were removed under vacuum and the residue treated with saturated NaCl (2 mL) and extracted with 4:1 EtOAc/iPrOH (x4). The organic fractions were combined, filtered and evaporated to give 115 mg of 1-(4-oxocyclohexyl)pyrrolidin-2-one.

Workup

  1. customreaction mixture
  2. concentrationwas concentrated in vacuo
  3. additiontreated with saturated NaHCO3 to pH 6
  4. customThe solvents were removed under vacuum
  5. additionthe residue treated with saturated NaCl (2 mL)
  6. extractionextracted with 4:1 EtOAc/iPrOH (x4)
  7. filtrationfiltered
  8. customevaporated

Sources & evidence

ORD record
ord-f8022aab41574e85bac03856e4ac8ad5
Source dataset
uspto-grants-2015_06
Patent number
US09062048B2

Reaction notes

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