Formaldehyde → (4S)-N-Boc-4-phenylmethyloxazolidin-5-one

HRID 1071875Notes

Reaction equation

HRID 1071875 reaction equation
[C:1]([O:5][C:6]([NH:8][C@H:9]([C:17]([OH:19])=[O:18])[CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH2:20]=O>C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1.C1(C)C=CC=CC=1>[C:1]([O:5][C:6]([N:8]1[C@@H:9]([CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:17](=[O:19])[O:18][CH2:20]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]

Participants

5

Reactant 2

HCID 712FormaldehydeHCID 77857L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-

Product 1

HCID 11482799(4S)-N-Boc-4-phenylmethyloxazolidin-5-oneYield 72.2%

Reagents, catalysts & solvents 2

HCID 466102Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)CatalystHCID 1140TolueneSolvent

Procedure

Tert-butoxycarbonyl-L-phenylalanine (20.00 g), paraformaldehyde (6.04 g) and pyridinium p-toluenesulfonate (0.95 g) were added to toluene (200 ml), and they were stirred under heating and reflux for 30 minutes. The reaction mixture was cooled to room temperature and washed with a saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution. The obtained toluene layer was dried over anhydrous sodium sulfate and then sodium sulfate was removed. The solvent was evaporated under reduced pressure. The concentrated solution was cooled to room temperature to crystallize the product. The crystals were separated and dried to obtain intended (4S)-N-tert-butoxycarbonyl-4-phenylmethyloxazolidin-5-one (15.10 g) (yield: 72%).

Workup

  1. temperatureunder heating
  2. temperaturereflux for 30 minutes
  3. washwashed with a saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution
  4. dry with materialThe obtained toluene layer was dried over anhydrous sodium sulfate
  5. customsodium sulfate was removed
  6. customThe solvent was evaporated under reduced pressure
  7. temperatureThe concentrated solution was cooled to room temperature
  8. customto crystallize the product
  9. customThe crystals were separated
  10. customdried

Sources & evidence

ORD record
ord-2d1a17c2b3c2412eaeb3989c14e5cfdf
Source dataset
uspto-grants-2005_06
Patent number
US06906224B2

Reaction notes

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