Hydrochloric Acid → 1,2-Dihydro-9-hydroxy-7-(3-methyl-2-octyl)-4-oxo-4H-thieno[2,3-c][1]benzopyran

HRID 1657650Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1657650
CO[C:3]([CH:5]1[C:9](=O)[CH2:8][S:7][CH2:6]1)=O.[CH3:11][CH:12]([CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH:13]([C:15]1[CH:16]=[C:17]([OH:22])C=[C:19]([CH:21]=1)[OH:20])[CH3:14].Cl.[CH2:29]([OH:31])C>>[OH:22][C:17]1[C:3]2[C:5]3[CH2:9][CH2:8][S:7][C:6]=3[C:29](=[O:31])[O:20][C:19]=2[CH:21]=[C:15]([CH:13]([CH:12]([CH3:11])[CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH3:14])[CH:16]=1

Komponenten

5

Edukt 4

HCID 313Hydrochloric AcidHCID 702EthanolHCID 984243-Thiophenecarboxylic acid, tetrahydro-4-oxo-, methyl esterHCID 2581765-(3-Methyloctan-2-yl)benzene-1,3-diol

Produkt 1

HCID 214339001,2-Dihydro-9-hydroxy-7-(3-methyl-2-octyl)-4-oxo-4H-thieno[2,3-c][1]benzopyran

Versuchsvorschrift

A solution of 20 g. (0.125 mole) of methyl-4-oxo-2,3,4,5-tetrahydrothiophene-3-carboxylate and 32 g. (0.135 mole of 5-(3-methyl-2-octyl)resorcinol in 200 ml. of absolute ethanol was cooled in an ice-salt bath and saturated with anhydrous hydrogen chloride. The reaction mixture was allowed to stand at room temperature for 72 hours and the solid which formed was removed by filtration. Recrystallization from ethanol gave 16 g. (37%) m.p. 165°-166°C. The structure was confirmed by infrared and nuclear magnetic resonance spectra.

Aufarbeitung

  1. customthe solid which formed
  2. customwas removed by filtration
  3. customRecrystallization from ethanol
  4. customgave 16 g

Quellen und Nachweise

ORD-Eintrag
ord-fc21f85face646cea39565899ce570d7
Quelldatensatz
uspto-grants-1976_06
Patentnummer
US03960871

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