Sodium Hydroxide → 3-Cyclopropyl-benzo[b]thiophene-2-carboxylic acid

HRID 2405875Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2405875
C([O:3][C:4]([C:6]1[S:10][C:9]2[CH:11]=[CH:12][CH:13]=[CH:14][C:8]=2[C:7]=1[CH:15]1[CH2:17][CH2:16]1)=[O:5])C.[OH-].[Na+]>C(O)C>[CH:15]1([C:7]2[C:8]3[CH:14]=[CH:13][CH:12]=[CH:11][C:9]=3[S:10][C:6]=2[C:4]([OH:5])=[O:3])[CH2:16][CH2:17]1

Komponenten

4

Edukt 2

HCID 14798Sodium HydroxideHCID 59651664HCID 59651664, Verbindung

Produkt 1

HCID 579205163-Cyclopropyl-benzo[b]thiophene-2-carboxylic acidAusbeute 79,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

A solution of compound 674-B (2.68 g, 10.9 mmol) in ethanol (30 mL) was treated with 3N aqueous sodium hydroxide (5.4 mL, 16.2 mmol) and refluxed for 2 h. The solution was cooled, and the solvent was evaporated in vacuo. The residue was dissolved in water and washed with dichloromethane. The aqueous phase was acidified with concentrated hydrochloric acid, and the product was extracted into ethyl acetate, washed with brine, dried over Na2SO4, filtered and the solvent was evaporated in vacuo, to afford 1.9 g of compound 674-C as a colorless solid. 1H-NMR (DMSO-d6): δ 0.58-1.37 (m, 4H), 2.44-2.47 (m, 1H), 7.13-7.61 (m, 2H), 7.98 (dd, 2H), 13.33 (br s, 1H).

Aufarbeitung

  1. temperaturerefluxed for 2 h
  2. temperatureThe solution was cooled
  3. customthe solvent was evaporated in vacuo
  4. dissolutionThe residue was dissolved in water
  5. washwashed with dichloromethane
  6. extractionthe product was extracted into ethyl acetate
  7. washwashed with brine
  8. dry with materialdried over Na2SO4
  9. filtrationfiltered
  10. customthe solvent was evaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-85f693c6488044c98cbad4d3f46c6e1c
Quelldatensatz
uspto-grants-2014_08
Patentnummer
US08809327B2

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