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Thionyl Chloride → Methyl (S)-(+)-4,5-dihydro-2-phenyl-4-oxazolecarboxylate

HRID 1794027
Notes
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Reaction equation

HRID 1794027 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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 24386Thionyl ChlorideHCID 2222571HCID 2222571, compound

Product 1

HCID 11074512Methyl (S)-(+)-4,5-dihydro-2-phenyl-4-oxazolecarboxylateYield 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).

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

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-1d6b6f5f23a2436d80fc92f96ab259aa
Source dataset
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07022722B2

Reaction notes

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