Hydrochloric Acid → 4-Bromo-2-propylthiophene

HRID 2258077

Reaktionsgleichung

Reaktionsgleichung von HRID 2258077
[Br:1][C:2]1[CH:3]=[C:4]([C:7](=O)[CH2:8][CH3:9])[S:5][CH:6]=1.O.NN.[OH-].[K+].Cl>C(O)CO.O>[Br:1][C:2]1[CH:3]=[C:4]([CH2:7][CH2:8][CH3:9])[S:5][CH:6]=1

Komponenten

7

Reaktionsbedingungen

Temperatur
160 °C

Versuchsvorschrift

To a solution of crude 1-(4-bromo-2-thienyl)-1-propanone, (53 g, 242 mmol, from step 1d above) in 210 mL of ethylene glycol was added hydrazine monohydrate (30 mL, 617 mmol). The resulting solution was then heated to 160° C. with stirring for 45 min. The solution was cooled to 35° C. and 42 g of KOH (750 mmol) was added. The mixture was heated to 160° C. and stirred for 1.5 hr. The reaction was cooled to room temperature, and 450 mL of water was added. The mixture was then acidified with conc. HCl, and the product was extracted with pentane (3×200mL). The pentane was dried over MgSO4, filtered and evaporated to yield 39.7 g of crude product as a free flowing oil. The material was purified by flash chromatography on silica gel, eluting with pentane, to afford 27 g, (54% yield) of the title product. b.p. 120°-125° C. @7 mm Hg. NMR (CDCl3) δ: 0.97 (t, 3H, J=7.5 Hz), 1.69 (sextet, 2H, J=7.5 Hz), 2.75 (t, 2H, J=7.5 Hz), 6.70 (d, 1H), 7.00 (d, 1H).

Aufarbeitung

  1. temperatureThe solution was cooled to 35° C.
  2. temperatureThe mixture was heated to 160° C.
  3. stirringstirred for 1.5 hr
  4. temperatureThe reaction was cooled to room temperature
  5. extractionthe product was extracted with pentane (3×200mL)
  6. dry with materialThe pentane was dried over MgSO4
  7. filtrationfiltered
  8. customevaporated
  9. customto yield 39.7 g of crude product as
  10. customThe material was purified by flash chromatography on silica gel
  11. washeluting with pentane

Quellen und Nachweise

ORD-Eintrag
ord-ba29929bf1a6475f9732d856c9347438
Quelldatensatz
uspto-grants-1997_08
Patentnummer
US05659037

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