Thionyl Chloride → Methyl (4S)-2-phenyl-4,5-dihydro-1,3-oxazole-4-carboxylate

HRID 1885032Notes

Reaction equation

HRID 1885032 reaction equation
[CH3:1][O:2][C:3](=[O:16])[C@H:4]([CH2:14][OH:15])[NH:5][C:6](=O)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.S(Cl)(Cl)=O>C(Cl)Cl>[C:7]1([C:6]2[O:15][CH2:14][C@@H:4]([C:3]([O:2][CH3:1])=[O:16])[N:5]=2)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1

Participants

4

Reactant 2

HCID 24386Thionyl ChlorideHCID 2222571HCID 2222571, compound

Product 1

HCID 11074512Methyl (4S)-2-phenyl-4,5-dihydro-1,3-oxazole-4-carboxylateYield 78.7%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

A stirred mixture of N-benzoyl-L-serine methyl ester (21.0 g), thionyl chloride (21.0 g), and methylene chloride (150 ml) is stirred at reflux for 1 hour. The solvent is evaporated and the residue is diluted with cold water. Neutralize with sodium bicarbonate, and extract with ethyl acetate. Purification on silica gel (250 g), eluting with methanol:methylene chloride (01:99), yields methyl (S)-2-phenyl-2-oxazoline-4-carboxylate (15.2 g).

Workup

  1. temperatureat reflux for 1 hour
  2. customThe solvent is evaporated
  3. additionthe residue is diluted with cold water
  4. extractionNeutralize with sodium bicarbonate, and extract with ethyl acetate
  5. customPurification on silica gel (250 g)
  6. washeluting with methanol:methylene chloride (01:99)

Sources & evidence

ORD record
ord-3a69ff186dd149349be8e1a849617472
Source dataset
uspto-grants-2004_07
Patent number
US06768008B2

Reaction notes

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