Nitrogen → HCID 22905873, Verbindung

HRID 2257252Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2257252
Br[C:2]1[CH:7]=[C:6](Br)[CH:5]=[C:4]([C:9]([CH3:12])([CH3:11])[CH3:10])[C:3]=1[O:13][CH2:14][CH2:15]Br.N#N.C([Li])CCC.CCCCCC.[NH4+].[Cl-]>O1CCCC1.CCCCCC.CO.CCOCC>[C:9]([C:4]1[C:3]2[O:13][CH2:14][CH2:15][C:2]=2[CH:7]=[CH:6][CH:5]=1)([CH3:12])([CH3:11])[CH3:10]

Komponenten

8

Versuchsvorschrift

A cold solution of 1,5-dibromo-2-(2-bromoethoxy)-3-tert-butylbenzene (5.00 g, 12.05 mmol) in tetrahydrofuran/hexane (100 mL/20 mL) is cooled to -95° C. (MeOH/Et2O, liquid N2). A solution of n-butyl lithium in hexane (12 mL, 30.1 mmol) is added dropwise, and the reaction is allowed to stir for 0.5 h between -95° C. and -80° C. After 4 h, the reaction is poured onto saturated NH4Cl, and extracted with ethylacetate. The organic layer is washed twice with H2O and once with brine. The combined organic layers are dried (MgSO4), filtered, and evaporated. The resulting oil is purified by chromatography over SiO2 using hexanes. The resulting oil is distilled at reduced pressure to give 7-tert-butyl-2,3-dihydrobenzo[b]furan as a low melting white solid.

Aufarbeitung

  1. waitAfter 4 h
  2. extractionextracted with ethylacetate
  3. washThe organic layer is washed twice with H2O and once with brine
  4. dry with materialThe combined organic layers are dried (MgSO4)
  5. filtrationfiltered
  6. customevaporated
  7. customThe resulting oil is purified by chromatography over SiO2
  8. distillationThe resulting oil is distilled at reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-a9f000b2544742d28babbda48987e172
Quelldatensatz
uspto-grants-1997_08
Patentnummer
US05656661

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