Thionyl Chloride → Methyl 1-chloroindan-4-carboxylate

HRID 1606721

Reaktionsgleichung

Reaktionsgleichung von HRID 1606721
O[CH:2]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([C:11]([O:13][CH3:14])=[O:12])[C:5]=2[CH2:4][CH2:3]1.S(Cl)([Cl:17])=O>>[Cl:17][CH:2]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([C:11]([O:13][CH3:14])=[O:12])[C:5]=2[CH2:4][CH2:3]1

Komponenten

3

Versuchsvorschrift

In 6 ml. of chllroform is dissolved 5.7 g. of methyl 1-hydroxyindan-4-carboxylate and, under cooling with ice, the solution is stirred. Then, 3 ml. of thionyl chloride is added dropwise and, after the dropwise addition has been completed, the mixture is further stirred under cooling with ice for one hour. Then, the solvent and the excess thionyl chloride are distilled off under reduced pressure. The residue obtained is purified by column chromatography on silica gel (500 g. silica gel; eluant: chloroform). The procedure gives methyl 1-chloroindan-4-carboxylate as an oily product.

Aufarbeitung

  1. dissolutionof chllroform is dissolved 5.7 g
  2. additionafter the dropwise addition
  3. stirringthe mixture is further stirred
  4. temperatureunder cooling with ice for one hour
  5. distillationThen, the solvent and the excess thionyl chloride are distilled off under reduced pressure
  6. customThe residue obtained
  7. customis purified by column chromatography on silica gel (500 g. silica gel; eluant: chloroform)

Quellen und Nachweise

ORD-Eintrag
ord-49d482482cf3431abc7d24e93cc534d1
Quelldatensatz
uspto-grants-1976_04
Patentnummer
US03953500

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