Sodium Carbonate → HCID 66666133, compound

HRID 2196305Notes

Reaction equation

HRID 2196305 reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([F:17])=[C:6]([C:8]2([CH2:15]O)[NH:13][C:12](=[O:14])[CH2:11][O:10][CH2:9]2)[CH:7]=1.C(N(S(F)(F)[F:24])CC)C.C([O-])([O-])=O.[Na+].[Na+]>C1COCC1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([F:17])=[C:6]([C:8]2([CH2:15][F:24])[NH:13][C:12](=[O:14])[CH2:11][O:10][CH2:9]2)[CH:7]=1

Participants

5

Reactant 3

HCID 10340Sodium CarbonateHCID 123472(Diethylamino)sulfur trifluorideHCID 66665931HCID 66665931, compound

Product 1

HCID 66666133HCID 66666133, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

To a solution of 5-(5-bromo-2-fluoro-phenyl)-5-hydroxymethyl-morpholin-3-one (1.6 g, 5.26 mmol) in 30 ml THF was added dropwise diethylaminosulfur trifluoride (0.97 ml, 7.34 mmol) and stirred for 2 h. The colorless solution was slowly added to an ice cooled Na2CO3 solution (10%,aqueous) and extracted with TBME. The organic layer was washed with brine, dried with MgSO4 and evaporated. The crude product was purified by chromatography on silica gel (heptane/EtOAc 3/1) to provide the title compound as a slightly yellow solid.

Workup

  1. extractionextracted with TBME
  2. washThe organic layer was washed with brine
  3. dry with materialdried with MgSO4
  4. customevaporated
  5. customThe crude product was purified by chromatography on silica gel (heptane/EtOAc 3/1)

Sources & evidence

ORD record
ord-8d58c32b069848ceaeb1e605d3866dbe
Source dataset
uspto-grants-2012_12
Patent number
US08338413B1

Reaction notes

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