Hydrochloric Acid → 2-Hydroxy-9-ethoxycarbonyl-10,11-dihydrodibenzo[b,f]thiepin

HRID 261550

Reaktionsgleichung

Reaktionsgleichung von HRID 261550
[OH:1][C:2]1[CH:19]=[CH:18][C:5]2[S:6][C:7]3[CH:14]=[CH:13][CH:12]=[C:11]([C:15]([OH:17])=[O:16])[C:8]=3[CH2:9][CH2:10][C:4]=2[CH:3]=1.Cl.[CH2:21](O)[CH3:22]>C(OCC)(=O)C.C1C=CC=CC=1>[OH:1][C:2]1[CH:19]=[CH:18][C:5]2[S:6][C:7]3[CH:14]=[CH:13][CH:12]=[C:11]([C:15]([O:17][CH2:21][CH3:22])=[O:16])[C:8]=3[CH2:9][CH2:10][C:4]=2[CH:3]=1

Komponenten

5

Versuchsvorschrift

An amount of 1.7 g of 2-hydroxy-9-carboxy-10,11-dihydrodibenzo[ b,f] thiepin was dissolved in 50 ml of anhydrous ethanol and the mixture was refluxed for 3 hours, while hydrogen chloride gas was bubbled into the mixture. The solvent was distilled off to obtain the residue which was dissolved in the mixed solvent of ethyl acetate-benzene. The solution was washed with saturated sodium chloride solution and freed of solvent by distillation to obtain 1.6 g (85%) of 2-hydroxy-9-ethoxycarbonyl-10,11-dihydrodibenzo[b,f]thiepin as brown crystals having a melting point of 125°-129° C.

Aufarbeitung

  1. customwas bubbled into the mixture
  2. distillationThe solvent was distilled off
  3. customto obtain the residue which
  4. washThe solution was washed with saturated sodium chloride solution
  5. distillationfreed of solvent by distillation

Quellen und Nachweise

ORD-Eintrag
ord-c5c03ba49e764c6689d82ebf3ba22f88
Quelldatensatz
uspto-grants-1979_08
Patentnummer
US04166127

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