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Acetic Acid → (4-Methylbiphenyl-3-yl)methanol

HRID 1883618
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1883618
[CH3:1][C:2]1[CH:9]=[CH:8][C:7]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:6][C:3]=1[CH:4]=[O:5].B.[Na].C(O)(=O)C>O1CCCC1.O.[OH-].[Na+]>[CH3:1][C:2]1[CH:9]=[CH:8][C:7]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:6][C:3]=1[CH2:4][OH:5]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 3

HCID 176Acetic AcidHCID 120565292-Methyl-5-phenylbenzaldehydeHCID 178418435HCID 178418435, Verbindung

Produkt 1

HCID 12056528(4-Methylbiphenyl-3-yl)methanol

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 962WaterLösungsmittelHCID 8028Tetrahydrofuran
Lösungsmittel
HCID 14798Sodium HydroxideLösungsmittel

Reaktionsbedingungen

Temperatur
17.5 °C

Versuchsvorschrift

123 g (625 mmol) of 2-methyl-5-phenylbenzaldehyde was dissolved in a mixture of 1.1 L of tetrahydrofuran and 110 ml of water, and to the resulted solution was dropped, at 15 to 20° C., a solution prepared by dissolving 7.7 g (203 mmol) of sodium boron hydride in 70 ml of a 0.1 wt % sodium hydroxide aqueous solution. After completion of dropping, the mixture was stirred for 4 hours at 15 to 20° C. To this reaction solution was dropped 10 g of glacial acetic acid at 20° C. or lower, and this was poured into ice water. The reaction solution was extracted with t-butyl methyl ether, the organic layer was washed with water, saturated sodium bicarbonate solution, then, saturated saline, dried over anhydrous magnesium sulfate, then, concentrated to obtain 121 of 2-methyl-5-phenylbenzyl alcohol.

Aufarbeitung

  1. additionto the resulted solution was dropped, at 15 to 20° C.
  2. customa solution prepared
  3. extractionThe reaction solution was extracted with t-butyl methyl ether
  4. washthe organic layer was washed with water, saturated sodium bicarbonate solution
  5. dry with materialsaturated saline, dried over anhydrous magnesium sulfate
  6. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-4bcacee149ec4da088bc4aad7a767d4a
Quelldatensatz
uspto-grants-2004_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06762197B2

Notizen zur Reaktion

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