Sodium Sulfide → Methyl 4,6-dihydrothieno[3,4-b]thiophene-2-carboxylate

HRID 242763Notes

Reaction equation

HRID 242763 reaction equation
[CH3:1][O:2][C:3]([C:5]1[S:6][C:7]([CH2:12]Cl)=[C:8]([CH2:10]Cl)[CH:9]=1)=[O:4].[S-2:14].[Na+].[Na+]>CO>[CH3:1][O:2][C:3]([C:5]1[S:6][C:7]2[CH2:12][S:14][CH2:10][C:8]=2[CH:9]=1)=[O:4]

Participants

4

Reactant 2

HCID 14804Sodium SulfideHCID 11096691Methyl 4,5-bis(chloromethyl)thiophene-2-carboxylate

Product 1

HCID 3441857Methyl 4,6-dihydrothieno[3,4-b]thiophene-2-carboxylateYield 50%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent2×

Procedure

A solution of 4.8 g (20 mmol) (2) in 240 mL methanol was heated up and kept mild boiling. Sodium sulfide solution (1.7 g, 22 mmol) in 160 mL methanol was added dropwise in 2 h. After cooling of the reaction mixture, the precipitate was filtered off. The solvent was removed by evaporation and the residue was washed by water. Column chromatography on silica gel using dichloromethane yielded the pure title compound as a white solid 2.0 g (50%). 1HNMR (CDCl3): δ 3.87 (3H, s), 4.05-4.06 (2H, t, J=3 Hz), 4.19-4.20 (2H, t, J=3 Hz), 7.48 (1H, s). 13CNMR (CDCl3): δ33.12, 33.47, 52.19, 127.90, 137.30, 143.90, 146.64, 162.51.

Workup

  1. temperatureAfter cooling of the reaction mixture
  2. filtrationthe precipitate was filtered off
  3. customThe solvent was removed by evaporation
  4. washthe residue was washed by water

Sources & evidence

ORD record
ord-3dd499004e4042c3a1599452eb6b739c
Source dataset
uspto-grants-2014_02
Patent number
US08653228B2

Reaction notes

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