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Water → HCID 20496709, Verbindung

HRID 1074443
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1074443
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][C:15](O)=[O:16])=[CH:6][CH:5]=1)([O-:3])=[O:2].O>O1CCCC1>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][OH:16])=[CH:8][CH:9]=1)([O-:3])=[O:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 962WaterHCID 204967086-(4-Nitrophenyl)hexanoic acid

Produkt 1

HCID 20496709HCID 20496709, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To a solution of 9.1 g of 6-(4-nitrophenyl)hexanoic acid in 200 ml of dried tetrahydrofuran was added, dropwise, a solution of borane-dimethyl sulfide complex (0.042 mole) in 40 ml of dried tetrahydrofuran. The resulting mixture was stirred at room temperature for 16 hours and then heated at reflux for 1 hour before it was cooled again to room temperature. Water (10 ml) was added, the mixture was stirred for 15 minutes, most of the solvent was removed, and water was added to the residue. The resultant aqueous mixture was extracted with diethyl ether and the extract was washed with aqueous saturated sodium bicarbonate solution, water, and aqueous saturated sodium chloride solution and dried over magnesium sulfate. The solvent was then evaporated to leave 6-(4-nitrophenyl)hexanol as a yellow oil.

Aufarbeitung

  1. temperatureheated
  2. temperatureat reflux for 1 hour before it
  3. temperaturewas cooled again to room temperature
  4. stirringthe mixture was stirred for 15 minutes, most of the solvent
  5. customwas removed
  6. additionwater was added to the residue
  7. extractionThe resultant aqueous mixture was extracted with diethyl ether
  8. washthe extract was washed with aqueous saturated sodium bicarbonate solution, water, and aqueous saturated sodium chloride solution
  9. dry with materialdried over magnesium sulfate
  10. customThe solvent was then evaporated

Quellen und Nachweise

ORD-Eintrag
ord-558e1882e01947e7a718a141a11336d6
Quelldatensatz
uspto-grants-1983_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04391818

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