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1-Bromo-4-iodobenzene → Tert-butyl 3-(4-bromophenyl)-3-hydroxypiperidine-1-carboxylate

HRID 1505918
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1505918
C([Li])CCC.[Br:6][C:7]1[CH:12]=[CH:11][C:10](I)=[CH:9][CH:8]=1.[C:14]([N:21]1[CH2:26][CH2:25][CH2:24][C:23](=[O:27])[CH2:22]1)([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15]>C1COCC1>[C:17]([O:16][C:14]([N:21]1[CH2:26][CH2:25][CH2:24][C:23]([C:10]2[CH:11]=[CH:12][C:7]([Br:6])=[CH:8][CH:9]=2)([OH:27])[CH2:22]1)=[O:15])([CH3:20])([CH3:18])[CH3:19]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 115221-Bromo-4-iodobenzeneHCID 2756825Tert-butyl 3-oxopiperidine-1-carboxylateHCID 178418339Butyllithium

Produkt 1

HCID 58266476Tert-butyl 3-(4-bromophenyl)-3-hydroxypiperidine-1-carboxylateAusbeute 56 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

n-Butyllithium (2.5 M in hexanes, 8.2 mL, 20.5 mmol) was added over 10 min to a solution of 1-bromo-4-iodobenzene (5.79 g, 20.5 mmol) in THF (100 mL) at −78° C. After 15 min, a solution of 1-boc-3-piperidone (3.71 g, 18.6 mmol) in THF (10 mL) was added and the resultant reaction mixture was left to stir at −78° C. for 1 h, then warmed to 0° C. and quenched by the addition of saturated aqueous ammonium chloride (50 mL). The mixture was allowed to warm to ambient temperature and partitioned between ethyl acetate (400 mL) and water (150 mL). The organic layer was separated, dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo. The resultant residue was purified by flash chromatography (silica, 80 g column, ISCO, 0-100% ethyl acetate in cyclohexane) to afford the title compound as a colourless gum (3.69 g, 56%). 1H NMR (CDCl3, 300 MHz): 7.52-7.46 (m, 2H); 7.42-7.36 (m, 2H); 4.16-3.87 (m, 2H); 3.13 (d, J=13.7 Hz, 1H); 2.92-2.77 (m, 1H); 2.03-1.53 (m, 4H); 1.47 (s, 9H).

Aufarbeitung

  1. customthe resultant reaction mixture
  2. waitwas left
  3. temperaturewarmed to 0° C.
  4. customquenched by the addition of saturated aqueous ammonium chloride (50 mL)
  5. temperatureto warm to ambient temperature
  6. custompartitioned between ethyl acetate (400 mL) and water (150 mL)
  7. customThe organic layer was separated
  8. dry with materialdried over anhydrous magnesium sulfate
  9. filtrationfiltered
  10. customevaporated in vacuo
  11. customThe resultant residue was purified by flash chromatography (silica, 80 g column, ISCO, 0-100% ethyl acetate in cyclohexane)

Quellen und Nachweise

ORD-Eintrag
ord-436ba52e0228451a81d06391249d3623
Quelldatensatz
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09216980B2

Notizen zur Reaktion

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