Hydrochloric Acid → 3-Phenyloxolan-2-one

HRID 1780212Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1780212
[C:1]1([C:7]([CH2:18][CH2:19][O:20][C:21](=[O:23])C)(C(OCC)=O)C(OCC)=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[Na+].Cl>CO>[C:1]1([CH:7]2[CH2:18][CH2:19][O:20][C:21]2=[O:23])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Komponenten

5

Versuchsvorschrift

The product of Example 2 (837 g, 2.6M) methanol (1.5 l) and 40% aq. NaOH (1 l, 10M) were heated to reflux for 2 hours. The reaction was then cooled to room temperature and acidified with conc. HCl (1l). The reaction was left as room temperature overnight and then extracted with methyl tert.butyl ether (1 l,500 ml). The extracts were washed with aq. Na2CO3, dried and evaporated to give the title compound(376 g, 89%).

Aufarbeitung

  1. temperatureto reflux for 2 hours
  2. extractionextracted with methyl tert.butyl ether (1 l,500 ml)
  3. washThe extracts were washed with aq. Na2CO3
  4. customdried
  5. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-7d238d5a0dac4316a959a22dd1e8cc7f
Quelldatensatz
uspto-grants-1997_05
Patentnummer
US05629432

Notizen zur Reaktion

Wird geladen…