Ammonium Chloride → Ethyl 5-amino-4-methoxythiophene-2-carboxylate

HRID 59754Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 59754
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[S:6][C:7]=1[N+:8]([O-])=O.[Cl-].[NH4+]>CCO.O.[Fe]>[NH2:8][C:7]1[S:6][C:5]([C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:4][C:3]=1[O:2][CH3:1]

Komponenten

5

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

A mixture of ethyl 4-methoxy-5-nitrothiophene-2-carboxylate (Int. 68) (300 mg, 1.297 mmol) (prepared as described in Step 4 hereabove reported), and ammonium chloride (139 mg, 2.59 mmol) in EtOH/water=2/1 (18 ml) was heated at 50° C. until complete dissolution. Iron powder (435 mg, 7.78 mmol) was added, and the reaction was heated at 80° C. for 2 hours. The mixture was filtered and the filtrate was concentrated under vacuum; the residue was portioned between brine and EtOAc and the organic phase was dried over sodium sulfate. The solvent was removed to afford ethyl 5-amino-4-methoxythiophene-2-carboxylate (Int. 69) in a mixture with approximately 30% of corresponding methyl ester (261 mg, 1.297 mmol, MS/ESI+201.9 [MH]+). This intermediate was used as such in the following step.

Aufarbeitung

  1. temperaturethe reaction was heated at 80° C. for 2 hours
  2. filtrationThe mixture was filtered
  3. concentrationthe filtrate was concentrated under vacuum
  4. dry with materialthe organic phase was dried over sodium sulfate
  5. customThe solvent was removed

Quellen und Nachweise

ORD-Eintrag
ord-1f953e59a22b4bf3927beb31b17e41b5
Quelldatensatz
uspto-grants-2016_09
Patentnummer
US09440954B2

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