Hydrochloric Acid → 3,5-Dimethylchlorobenzene

HRID 326996

Reaktionsgleichung

Reaktionsgleichung von HRID 326996
[CH3:1][C:2]1[CH:3]=[C:4]([CH:6]=[C:7]([CH3:9])[CH:8]=1)N.[ClH:10].N([O-])=O.[Na+]>O.[Cu]Cl>[CH3:1][C:2]1[CH:3]=[C:4]([Cl:10])[CH:6]=[C:7]([CH3:9])[CH:8]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
-10 °C

Versuchsvorschrift

A total of 33.0 g of 3,5-dimethylaniline was added dropwise over 20 minutes to 200 ml of concentrated hydrochloric acid at such a rate that the temperature of the reaction was kept below 35° C. After several minutes of vigorous stirring, the reaction was cooled to -10° C. A solution of 19.7 g of sodium nitrite dissolved in 50 ml of water was added dropwise over 30 minutes at such a rate that the reaction temperature was kept between -12° C. to -16° C. Then, 3.0 g of copper (I) chloride was added and the reaction was warmed to 27° C. At this temperature foaming was noted and the reaction temperature was maintained below 35° C. with an ice water bath. After one hour, the reaction was poured onto 350 g of ice. Once the ice melted the crude product was extracted with 400 ml of hexanes, the organic phase was dried with magnesium sulfate, filtered, and concentrated to yield 20.2 g of a liquid. This material was diluted with 5 ml of hexanes and chromatographed on neutral alumina (Brockman 1, 150 mesh), eluting with 1200 ml of hexanes and collecting 200 ml fractions. The desired 95% pure intermediate, 10.1 g, was isolated cleanly in fractions 1 and 2.

Aufarbeitung

  1. customwas kept below 35° C
  2. waitAfter several minutes of vigorous stirring
  3. additionwas added dropwise over 30 minutes at such a rate that the reaction temperature
  4. customwas kept between -12° C. to -16° C
  5. temperaturethe reaction was warmed to 27° C
  6. temperaturethe reaction temperature was maintained below 35° C. with an ice water bath
  7. extractionwas extracted with 400 ml of hexanes
  8. dry with materialthe organic phase was dried with magnesium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-250b93718ac24c5296f505d39c386af2
Quelldatensatz
uspto-grants-1993_12
Patentnummer
US05272128

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