Reaktion #1563903

ord-0f088a84fcce41baaa2729bc13579dee

Reaktionsgleichung

Oc1ccccc1O
catechol
COC(C)(C)OC
2,2-Dimethoxypropane
O=C([O-])O.[Na+]
NaHCO3
CC1(C)Oc2ccccc2O1
2,2-dimethylbenzo[d][1,3]dioxole
Ausbeute 18.9%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturat reflux for 6 h
  2. 2
    SonstigeAfter reaction
  3. 3
    SonstigeThe solvent was removed
  4. 4
    workup.DISTILLATIONthe residue was purified by distillation under reduced pressure at 36° C.

Vorschrift

A mixture of catechol (10 g, 91 mmol), 2,2-Dimethoxypropane (8.6 g, 82.6 mmol) and p-TsOH (33 mg, 0.17 mmol) in toluene (100 ml) was stirred at reflux for 6 h. After reaction, the mixture was cooled to room temperature and NaHCO3 was added to neutralize the mixture. The solvent was removed and the residue was purified by distillation under reduced pressure at 36° C. to obtain 2,2-dimethylbenzo[d][1,3]dioxole (2.34 g, 17%) as a yellow oil. 1H NMR (CDCl3-d6) δ 1.69 (s, 6H), 6.78 (m, 4H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09402832B2uspto-grants-2016_08