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Benzene → 3,4,4-Trimethoxy-1-(phenylmethyl)piperidine ethanedioate

HRID 1088355
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1088355
[CH3:1][O:2][C:3]1([O:17][CH3:18])[CH2:8][CH2:7][N:6]([CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH2:5][CH:4]1[OH:16].[OH-].[Na+].[CH:21]1C=CC=CC=1.S(OC)(OC)(=O)=[O:28]>[Cl-].C([N+](CC)(CC)CC1C=CC=CC=1)C.O>[C:4]([OH:28])(=[O:16])[C:3]([OH:17])=[O:2].[CH3:21][O:16][CH:4]1[C:3]([O:17][CH3:18])([O:2][CH3:1])[CH2:8][CH2:7][N:6]([CH2:9][C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH2:5]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 241BenzeneHCID 6497Dimethyl Sulfate2×HCID 14798Sodium HydroxideHCID 30192741-Benzyl-4,4-dimethoxypiperidin-3-ol

Produkt 1

HCID 867442673,4,4-Trimethoxy-1-(phenylmethyl)piperidine ethanedioate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 66133
Benzyl triethylammonium chloride
Katalysator
HCID 962WaterLösungsmittel

Versuchsvorschrift

To a stirred mixture of 85 parts of 4,4-dimethoxy-1-(phenylmethyl)-3-piperidinol and 480 parts of sodium hydroxide solution 60% were added 288 parts of benzene and 0.5 parts of N,N,N-triethylbenzenemethanaminium chloride. Then there were added dropwise 49.2 parts of dimethyl sulfate at a temperature below 30° C. After stirring overnight at room temperature, there was added another portion of 13.3 parts of dimethyl sulfate and stirring was continued for 4 hours at room temperature. The reaction mixture was cooled, 640 parts of water were added and the layers were separated. The aqueous phase was extracted with benzene. The formed suspension was filtered and the filter-cake was set aside. The combined organic phases were washed with water, dried, filtered and evaporated. The oily residue was distilled (bp. 138° C. at 1 mm. pressure). The distillate was converted into the ethanedioate salt in 2-propanol. The salt was filtered off and crystallized from ethanol, yielding 34.9 parts of 3,4,4-trimethoxy-1-(phenylmethyl)piperidine ethanedioate; mp. 180.6° C. (intermediate 58).

Aufarbeitung

  1. stirringstirring
  2. waitwas continued for 4 hours at room temperature
  3. temperatureThe reaction mixture was cooled
  4. customthe layers were separated
  5. extractionThe aqueous phase was extracted with benzene
  6. filtrationThe formed suspension was filtered
  7. washThe combined organic phases were washed with water
  8. customdried
  9. filtrationfiltered
  10. customevaporated
  11. distillationThe oily residue was distilled (bp. 138° C. at 1 mm. pressure)
  12. filtrationThe salt was filtered off
  13. customcrystallized from ethanol

Quellen und Nachweise

ORD-Eintrag
ord-99d6d9fea3f240eca07448754c3e1a66
Quelldatensatz
uspto-grants-1990_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04962115

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