Hydrochloric Acid → 5-(Chloromethyl)-6-propyl-1,3-benzodioxole

HRID 1195281

Reaktionsgleichung

Reaktionsgleichung von HRID 1195281
CCCCOCCOCCO[CH2:12][C:13]1[CH:14]=[C:15]2[O:24][CH2:23][O:22][C:16]2=[CH:17][C:18]=1[CH2:19][CH2:20][CH3:21].[ClH:25].O>C1C=CC=CC=1>[CH2:19]([C:18]1[C:13]([CH2:12][Cl:25])=[CH:14][C:15]2[O:24][CH2:23][O:22][C:16]=2[CH:17]=1)[CH2:20][CH3:21]

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 962WaterHCID 5794Piperonyl Butoxide

Produkt 1

HCID 747395-(Chloromethyl)-6-propyl-1,3-benzodioxole

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 241BenzeneLösungsmittel

Versuchsvorschrift

15 g of piperonyl butoxide and 300 ml of concentrated hydrochloric acid were dissolved in 100 ml of benzene and the solution was heated under reflux for 3 h. The reaction mixture was cooled to room temperature and water was added thereto. After extraction with ethyl acetate, the extract was washed with water, dried over magnesium sulfate and concentrated under reduced pressure to obtain 12 g of 6-propyl-5-chloromethyl-1,3-benzodioxole in the form of a faint brown oil.

Aufarbeitung

  1. temperaturethe solution was heated
  2. temperatureunder reflux for 3 h
  3. extractionAfter extraction with ethyl acetate
  4. washthe extract was washed with water
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-1278d1fec602435a80145e076215f150
Quelldatensatz
uspto-grants-1992_05
Patentnummer
US05110956

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