Potassium Carbonate → HCID 70543145, Verbindung

HRID 1856538Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1856538
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][C:8]3[CH:10]=[C:11]([CH2:14][C:15]([OH:17])=[O:16])[CH:12]=[CH:13][C:7]=3[C:6]=2[CH:18]=1.C(=O)([O-])[O-].[K+].[K+].Cl.[CH3:26][N:27]([CH2:29][CH2:30]Cl)[CH3:28]>CN(C)C=O>[ClH:1].[CH3:26][N:27]([CH3:28])[CH2:29][CH2:30][O:16][C:15](=[O:17])[CH2:14][C:11]1[CH:12]=[CH:13][C:7]2[C:6]3[CH:18]=[C:2]([Cl:1])[CH:3]=[CH:4][C:5]=3[S:9][C:8]=2[CH:10]=1

Komponenten

5

Versuchsvorschrift

A mixture of 2.76 g. of 8-chlorodibenzothiophene-3-acetic acid, 3.04 g. of potassium carbonate, 1.73 g. of dimethylaminoethyl chloride hydrochloride, and 250 ml. of dimethylformamide was stirred and heated at 120° for 4 hours. The solvent was removed in vacuo on the steam bath, and 75 ml. of water added to the residue. The oil was extracted with ethyl acetate and the crude product precipitated as the hydrochloride by the addition of hydrogen chloride. On crystallization from acetone, 1.5 g. of 8-chlorodibenzothiophene-3-acetic acid 2-dimethylaminoethyl ester hydrochloride, m.p. 179°-181°, was obtained.

Aufarbeitung

  1. additionA mixture of 2.76 g
  2. temperatureheated at 120° for 4 hours
  3. customThe solvent was removed in vacuo on the steam bath, and 75 ml
  4. additionof water added to the residue
  5. extractionThe oil was extracted with ethyl acetate
  6. customthe crude product precipitated as the hydrochloride by the addition of hydrogen chloride
  7. customOn crystallization from acetone, 1.5 g

Quellen und Nachweise

ORD-Eintrag
ord-ecc3509f32f54c7d97ec86aa4e03c62b
Quelldatensatz
uspto-grants-1980_08
Patentnummer
US04219657

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