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Hydrochloric Acid → 1-Benzyl-4-(4-phenylbutylidene)piperidine

HRID 278204
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 278204
C1COCC1.[Br-].[C:7]1([CH2:13][CH2:14][CH2:15][CH2:16][P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[CH2:36]([N:43]1[CH2:48][CH2:47][C:46](=O)[CH2:45][CH2:44]1)[C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1.Cl>C1(C)C=CC=CC=1>[CH2:36]([N:43]1[CH2:48][CH2:47][C:46](=[CH:16][CH2:15][CH2:14][CH2:13][C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH2:45][CH2:44]1)[C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 313Hydrochloric AcidHCID 8028TetrahydrofuranHCID 192201-Benzyl-4-piperidoneHCID 18187515(4-Phenylbutyl)triphenylphosphonium bromide

Produkt 1

HCID 181876891-Benzyl-4-(4-phenylbutylidene)piperidineAusbeute 58,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140
Toluene
Lösungsmittel
3×

Versuchsvorschrift

A 0.62M solution of potassium bis(trimethylsilyl)aride in THF (180 mL, 112 mmol) in toluene (250 mL) was added to a mixture of (4-phenylbut-1-yl)triphenylphosphonium bromide from Step B (53 g) in toluene (250 mL) in an ice bath over 15 min with stirring under nitrogen. After stirring for a further 15 min, a solution of 1-benzyl4-piperidone (16.9 g) in toluene (100 mL) was added over 30 min with stirring. The reaction mixture was allowed to warm to rt over 15 h. The reaction mixture was then poured into cold 1N HCl (400 mL) and the layers were separated. The organic layer was extracted with two more portions of 1N HCl. The combined cloudy HCl solution and an oil layer in between were washed with toluene (200 mL) before the aqueous layer was basified by the addition of potassium hydroxide (30 g). The aqueous layer was extracted with ether (3×150 mL) and the combined organic layers were washed with water and brine, dried over sodium sulfate and concentrated. The crude product was purified by FC (10-15% ethyl acetate in hexanes having 4% (v/v) TEA) to give the title compound (16 g) as a colorless oil.

Aufarbeitung

  1. stirringAfter stirring for a further 15 min
  2. stirringwith stirring
  3. customthe layers were separated
  4. extractionThe organic layer was extracted with two more portions of 1N HCl
  5. washThe combined cloudy HCl solution and an oil layer in between were washed with toluene (200 mL) before the aqueous layer
  6. additionwas basified by the addition of potassium hydroxide (30 g)
  7. extractionThe aqueous layer was extracted with ether (3×150 mL)
  8. washthe combined organic layers were washed with water and brine
  9. dry with materialdried over sodium sulfate
  10. concentrationconcentrated
  11. customThe crude product was purified by FC (10-15% ethyl acetate in hexanes having 4% (v/v) TEA)

Quellen und Nachweise

ORD-Eintrag
ord-d2c61d71a6e64c62a39cde3692626ae5
Quelldatensatz
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06358979B1

Notizen zur Reaktion

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