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Water → Benzenemethanol,2-hydroxy-3,5-dimethyl-

HRID 2380655
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2380655
BrCCCC[CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].[OH-:11].[Na+].[CH:13](O)([CH3:15])[CH3:14].[OH2:17].[CH3:18]CCCCC>>[OH:11][CH2:14][C:13]1[CH:15]=[C:9]([CH3:10])[CH:8]=[C:7]([CH3:6])[C:18]=1[OH:17]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 5

HCID 962WaterHCID 3776IsopropanolHCID 8058HexaneHCID 127421-BromononaneHCID 14798Sodium Hydroxide

Produkt 1

HCID 11480550Benzenemethanol,2-hydroxy-3,5-dimethyl-Ausbeute 50,5 %

Versuchsvorschrift

A 250-mL round-bottom flask equipped with a magnetic stirrer, condenser, and Ar-inlet tube was charged with 22.0 g (145 mmol) of crude (1), 24.7 mL (130 mmol) of 1-bromononane (Fluka), 5.79 (145 mmol) of sodium hydroxide (Fisher), and 100 mL of isopropanol (Fisher). After the mixture was refluxed overnight, 100 mL of water and 100 mL of hexane (Fisher) were added. The hexane layer was washed with 20 mL of 1N NaOH (Fisher). The combined aqueous layers were extracted with 50 mL of hexane. Then, the combined hexane solutions were extracted with 100 mL+2×50 mL=200 mL of 95% methanol. The combined methanol extracts were concentrated. The residual water was removed azeotropically with 100 mL of toluene. The residue was dried at 50° C. under high vacuum to give 28.1 g of crude (2) as a brown oil; 50.5% yield from (1), 77.7% yield based on 1-bromononane.

Aufarbeitung

  1. customA 250-mL round-bottom flask equipped with a magnetic stirrer, condenser
  2. temperatureAfter the mixture was refluxed overnight
  3. washThe hexane layer was washed with 20 mL of 1N NaOH (Fisher)
  4. extractionThe combined aqueous layers were extracted with 50 mL of hexane
  5. extractionThen, the combined hexane solutions were extracted with 100 mL+2×50 mL=200 mL of 95% methanol
  6. concentrationThe combined methanol extracts were concentrated
  7. customThe residual water was removed azeotropically with 100 mL of toluene
  8. customThe residue was dried at 50° C. under high vacuum

Quellen und Nachweise

ORD-Eintrag
ord-b2229f15354a4c5983ad347380e1ee0c
Quelldatensatz
uspto-grants-1994_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05369126

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