Dimethylformamide → HCID 13290046, Verbindung

HRID 1903493Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1903493
[Cl:1][C:2]1[C:3]([OH:16])=[CH:4][C:5]2[CH:9]=[C:8]([CH:10]([CH2:12][CH3:13])[OH:11])[S:7][C:6]=2[C:14]=1[Cl:15].Br[CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20].C(=O)([O-])[O-].[K+].[K+].CN(C)C=O>CC(=O)CC>[CH2:22]([O:21][C:19](=[O:20])[CH2:18][O:16][C:3]1[C:2]([Cl:1])=[C:14]([Cl:15])[C:6]2[S:7][C:8]([CH:10]([OH:11])[CH2:12][CH3:13])=[CH:9][C:5]=2[CH:4]=1)[CH3:23]

Komponenten

6

Versuchsvorschrift

To a mixture of 6,7-dichloro-5-hydroxy-α-ethylbenzo[b]thiophene-2-methanol and 200 ml of 2-butanone is added a mixture of 7.35 g of ethyl bromoacetate in 100 ml of 2-butanone, followed by 7.4 g of potassium carbonate and 3.3 ml of sieve-dried dimethylformamide. The reaction mixture is stirred at 95°-100° for 3 hrs, allowed to cool and filtered. To the filtrate is added 100 ml of water and the mixture is extracted with ethyl ether. The organic layers are washed, dried over anhydrous magnesium sulfate, filtered and the solvent removed to give an oil which solidifies on cooling. Recrystallization from ethyl ether and hexane gives 10 g of ethyl[ (6,7-dichloro-2-(1-hydroxypropyl]benzo[b]thien-5-yl]oxy]acetate, mp 69°-70°.

Aufarbeitung

  1. additionis added
  2. temperatureto cool
  3. filtrationfiltered
  4. additionTo the filtrate is added 100 ml of water
  5. extractionthe mixture is extracted with ethyl ether
  6. washThe organic layers are washed
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. customthe solvent removed
  10. customto give an oil which
  11. temperatureon cooling
  12. customRecrystallization from ethyl ether and hexane

Quellen und Nachweise

ORD-Eintrag
ord-69d51c6befcd48ec9ec434e069c8b343
Quelldatensatz
uspto-grants-1984_03
Patentnummer
US04436748

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