Bromotrichloromethane → Methyl 2-(3-chlorophenyl)-1,3-oxazole-4-carboxylate

HRID 273139Notes

Reaction equation

HRID 273139 reaction equation
[CH3:1][O:2][C:3](=[O:17])[CH:4]([NH:7][C:8](=[O:16])[C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([Cl:15])[CH:10]=1)[CH2:5]O.BrC(Cl)(Cl)Cl.C1CCN2C(=NCCC2)CC1>C(Cl)Cl>[CH3:1][O:2][C:3]([C:4]1[N:7]=[C:8]([C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([Cl:15])[CH:10]=2)[O:16][CH:5]=1)=[O:17]

Participants

5

Reactant 3

HCID 6383BromotrichloromethaneHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 43405659HCID 43405659, compound

Product 1

HCID 21681350Methyl 2-(3-chlorophenyl)-1,3-oxazole-4-carboxylateYield 59%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of 2-(3-chloro-benzoylamino)-3-hydroxy-propionic acid methyl ester (7.2 g, 29.6 mmol) in CH2Cl2 at −20° C. was added dropwise De-oxofluor (7.2 g, 32.6 mmol). After stirring at this temperature for 30 min, BrCCl3 (3.6 g, 18.1 mmol) was added dropwise followed by DBU (2.79 g, 18.1 mmol). The mixture was then stirred at 2-3° C. for 8 h ad then quenched with saturated NaHCO3 followed by extraction with ethyl acetate. The organic extract as then washed with brine and dried over Na2SO4 (anhydrous). Purification was performed by flash column chromatography on silica gel using ethyl acetate in hexanes as eluant to afford 2-(3-chloro-phenyl)-oxazole-4-carboxylic acid methyl ester (4.1 g, 59%) as a yellow solid. 1H NMR (CDCl3) d (ppm): 8.30 (s, 1 H), 8.12 (d, 1 H), 7.98 (dd, 1 H), 7.45 (m, 2 H), 3.96 (s, 3 H).

Workup

  1. stirringThe mixture was then stirred at 2-3° C. for 8 h ad
  2. customthen quenched with saturated NaHCO3
  3. extractionfollowed by extraction with ethyl acetate
  4. extractionThe organic extract
  5. washas then washed with brine
  6. dry with materialdried over Na2SO4 (anhydrous)
  7. customPurification

Sources & evidence

ORD record
ord-6ee25507002d413a93eff7fbb866a529
Source dataset
uspto-grants-2008_11
Patent number
US07456200B2

Reaction notes

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