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Triphenylphosphine → Tert-butyl 4-(2-(4-bromo-2-(trifluoromethyl)phenoxy)ethyl)piperidine-1-carboxylate

HRID 517937
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 517937
CC(OC(/N=N/C(OC(C)C)=O)=O)C.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Br:34][C:35]1[CH:40]=[CH:39][C:38]([OH:41])=[C:37]([C:42]([F:45])([F:44])[F:43])[CH:36]=1.O[CH2:47][CH2:48][CH:49]1[CH2:54][CH2:53][N:52]([C:55]([O:57][C:58]([CH3:61])([CH3:60])[CH3:59])=[O:56])[CH2:51][CH2:50]1>C(Cl)Cl>[Br:34][C:35]1[CH:40]=[CH:39][C:38]([O:41][CH2:47][CH2:48][CH:49]2[CH2:50][CH2:51][N:52]([C:55]([O:57][C:58]([CH3:59])([CH3:61])[CH3:60])=[O:56])[CH2:53][CH2:54]2)=[C:37]([C:42]([F:43])([F:44])[F:45])[CH:36]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 11776TriphenylphosphineHCID 142784o-Cresol, 4-bromo-alpha,alpha,alpha-trifluoro-HCID 8541401-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidineHCID 5363146Diisopropyl azodicarboxylate

Produkt 1

HCID 67294273Tert-butyl 4-(2-(4-bromo-2-(trifluoromethyl)phenoxy)ethyl)piperidine-1-carboxylate

Reagenzien, Katalysatoren, Lösungsmittel

1
HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

DIAD (33.5 g) was added dropwise to the solution of triphenylphosphine (43.5 g), 4-bromo-2-trifluoromethylphenol (40 g) and tert-butyl 4-(2-hydroxyethyl)-piperidine-1-carboxylate (31.7 g) in DCM (200 ml) at 0° C. during 15 minutes. The mixture was then stirred at room temperature for 20 hours. After removal of DCM under reduced pressure, to the residue was added ether (100 ml) and heptane (300 ml), solid was then filtered off. Filtrate was then washed with 1M sodium hydroxide (100 ml×3). Organic layer dried over sodium sulphate, solvent removed under vacuum, residue was then columned on silica gel using heptane:EtOAc (5:1) as eluant to give tert-butyl 4-(2-(4-bromo-2-(trifluoromethyl)phenoxy)ethyl)piperidine-1-carboxylate as a colorless oil as product (61.3 g).

Aufarbeitung

  1. customAfter removal of DCM under reduced pressure
  2. additionto the residue was added ether (100 ml) and heptane (300 ml), solid
  3. filtrationwas then filtered off
  4. washFiltrate was then washed with 1M sodium hydroxide (100 ml×3)
  5. dry with materialOrganic layer dried over sodium sulphate, solvent
  6. customremoved under vacuum, residue

Quellen und Nachweise

ORD-Eintrag
ord-397246aa07b34753bc7c02ee9f38aeec
Quelldatensatz
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09115126B2

Notizen zur Reaktion

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