Nitrogen → 5-Methylsulfanylfuran-2-carboxylic acid ethyl ester

HRID 42765Notes

Reaction equation

HRID 42765 reaction equation
N#N.[CH2:3]([O:5][C:6]([C:8]1[O:9][C:10]([N+]([O-])=O)=[CH:11][CH:12]=1)=[O:7])[CH3:4].[CH3:16][S-:17].[Na+].[NH4+].[Cl-]>CS(C)=O>[CH2:3]([O:5][C:6]([C:8]1[O:9][C:10]([S:17][CH3:16])=[CH:11][CH:12]=1)=[O:7])[CH3:4]

Participants

6

Conditions

Temperature
100 °C

Procedure

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of commercially available 5-nitro-furan-2-carboxylic acid ethyl ester (5.00 g, 27.01 mmol) in DMSO (34.5 mL) was treated at rt with sodium methanethiolate (2.05 g 27.82 mmol). The mixture was then stirred overnight at 100° C., treated at rt with sat. aq. NH4Cl (250 mL) and the aqueous layer was extracted with EA (3×100 mL). The combined org. extracts were washed with sat. aq. NaHCO3 (100 mL) and brine (100 mL), dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (70:30 hept-EA) gave the title compound: TLC:rf (70:30 hept-EA)=0.52. LC-MS-conditions 02: tR=0.96 min; [M+AcCN+N+H]+=228.23.

Workup

  1. extractionthe aqueous layer was extracted with EA (3×100 mL)
  2. washextracts were washed with sat. aq. NaHCO3 (100 mL) and brine (100 mL)
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. customthe solvents were removed under reduced pressure
  6. customPurification of the residue by FC (70:30 hept-EA)

Sources & evidence

ORD record
ord-972af442c25840adac9ba8d17d63a670
Source dataset
uspto-grants-2013_09
Patent number
US08536209B2

Reaction notes

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