Hydrochloric Acid → HCID 59547213, compound

HRID 2408956Notes

Reaction equation

HRID 2408956 reaction equation
[CH3:1][C:2]1[Se:6][C:5]([C:7]([O:9][CH3:10])=[O:8])=[CH:4][C:3]=1[N+:11]([O-])=O.Cl.[Cl-].[NH4+]>O.CO.[Fe]>[NH2:11][C:3]1[CH:4]=[C:5]([C:7]([O:9][CH3:10])=[O:8])[Se:6][C:2]=1[CH3:1]

Participants

7

Procedure

To a solution of methyl 5-methyl-4-nitroselenophene-2-carboxylate (2.3 g, 9.28 mmol) in a mixture of water (5 mL) and methanol (40 mL) was added conc. hydrochloric acid (1.0 mL). To the above solution was added iron powder (2.6 g, 46.4 mmol) followed by ammonium chloride (2.5 g, 46.4 mmol) at rt. The reaction mixture was refluxed for 1 h and was then allowed to cool to rt. The solution was filtered and basified with saturated sodium bicarbonate solution. The solution was extracted with ethyl acetate (4×100 mL) and the combined organic layer was dried over sodium sulfate and filtered. Solvent was evaporated and the residue was chromatographed over silica gel column using hexane-ethyl acetate (80:20) as eluent to give methyl 4-amino-5-methylselenophene-2-carboxylate (1.6 g, 79%), mp 66-68° C. 1H NMR (400 MHz, DMSO-d6): δ 7.57 (1H, s), 4.72 (2H, br s), 3.73 (3H, s), 2.24 (3H, s).

Workup

  1. temperatureThe reaction mixture was refluxed for 1 h
  2. filtrationThe solution was filtered
  3. extractionThe solution was extracted with ethyl acetate (4×100 mL)
  4. dry with materialthe combined organic layer was dried over sodium sulfate
  5. filtrationfiltered
  6. customSolvent was evaporated
  7. customthe residue was chromatographed over silica gel column

Sources & evidence

ORD record
ord-4e0fe5d4c4844ab3a2a94f1e61379192
Source dataset
uspto-grants-2014_08
Patent number
US08815879B2

Reaction notes

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