Ammonium Chloride → HCID 69733599, Verbindung

HRID 1062503Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1062503
Br[CH2:2][CH:3]1[CH2:8][CH:7]2[CH2:9][CH:4]1[CH:5]=[CH:6]2.[CH2:10]([O:12][CH:13](OCC)[CH:14]=[CH2:15])[CH3:11].[Cl-].[NH4+]>O1CCCC1.[Cu]Br>[CH2:10]([O:12][CH:13]=[CH:14][CH2:15][CH2:2][CH:3]1[CH2:8][CH:7]2[CH2:9][CH:4]1[CH:5]=[CH:6]2)[CH3:11]

Komponenten

6

Edukt 3

HCID 25517Ammonium ChlorideHCID 624773,3-Diethoxy-1-propeneHCID 27760625-(bromomethyl)bicyclo[2.2.1]hept-2-ene

Produkt 1

HCID 69733599HCID 69733599, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 24593copper(I) bromideKatalysatorHCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

A Grignard reagent was customarily prepared from 200 g of 5-bromomethyl-2-norbornene in 500 ml of dry tetrahydrofuran. The Grignard reagent was added dropwise over one hour to a mixture of 130 g of 3,3-diethoxy-1-propene, 1.0 g of copper (I) bromide and 300 ml of dry tetrahydrofuran at 20° C. Stirring was continued for 20 hours whereupon the reaction solution was added to a saturated aqueous solution of ammonium chloride to stop reaction. After hexane extraction, the organic layer was successively washed with water, saturated sodium bicarbonate water and saturated sodium chloride water, dried over anhydrous sodium sulfate, and concentrated in vacuum, yielding 5-(4-ethoxy-3-buten-1-yl)-2-norbornene.

Aufarbeitung

  1. customreaction
  2. extractionAfter hexane extraction
  3. washthe organic layer was successively washed with water, saturated sodium bicarbonate water and saturated sodium chloride water
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated in vacuum

Quellen und Nachweise

ORD-Eintrag
ord-7bc15910770f4791a81eee156b66be35
Quelldatensatz
uspto-grants-2005_11
Patentnummer
US06962767B2

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