Potassium bisulfate → tert-Butyl (4-oxopentyl)carbamate

HRID 1004257Notes

Reaction equation

HRID 1004257 reaction equation
[C:1]([O:5][C:6](=[O:17])[NH:7][CH2:8][CH2:9][CH2:10][C:11](=[O:16])N(OC)C)([CH3:4])([CH3:3])[CH3:2].[CH3:18][Mg]Br.OS([O-])(=O)=O.[K+]>C1COCC1>[C:1]([O:5][C:6](=[O:17])[NH:7][CH2:8][CH2:9][CH2:10][C:11](=[O:16])[CH3:18])([CH3:2])([CH3:3])[CH3:4]

Participants

5

Reactant 3

HCID 516920Potassium bisulfateHCID 23112516tert-butyl N-(3-(methoxy(methyl)carbamoyl)propyl)carbamateHCID 178418573HCID 178418573, compound

Product 1

HCID 21478928tert-Butyl (4-oxopentyl)carbamate

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

To a stirred solution of 11-3 (10.0 g, 40.5 mmol) and THF (200 ml) at 0° C. was added methylmagnesium bromide (27.0 ml, 91.0 mmol; 3M in ether) dropwise over 20 minutes. After 2.0 hours, 10% KHSO4 was added slowly. The mixture was extracted with EtOAc. The organic portion was washed with sat. NaHCO3, brine, and dried over MgSO4. Evaporative removal of the solvent gave 11-4 as a colorless oil.

Workup

  1. extractionThe mixture was extracted with EtOAc
  2. washThe organic portion was washed with sat. NaHCO3, brine
  3. dry with materialdried over MgSO4
  4. customEvaporative removal of the solvent

Sources & evidence

ORD record
ord-586ef15237fd46e596813bed9e2f94da
Source dataset
uspto-grants-2000_04
Patent number
US06048861

Reaction notes

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