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Water → 2H-Pyran, 3,4-dihydro-6-[(phenylmethoxy)methyl]-

HRID 414774
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 414774
[OH:1][CH2:2][C:3]1[O:8][CH2:7][CH2:6][CH2:5][CH:4]=1.[H-].[Na+].[CH2:11](Cl)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.O>CN(C)C=O>[CH2:11]([O:1][CH2:2][C:3]1[O:8][CH2:7][CH2:6][CH2:5][CH:4]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 962WaterHCID 7503Benzyl ChlorideHCID 24758Sodium hydrideHCID 12511647(3,4-Dihydro-2H-pyran-6-yl)methanol

Produkt 1

HCID 113561752H-Pyran, 3,4-dihydro-6-[(phenylmethoxy)methyl]-Ausbeute 92 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228
Dimethylformamide
Lösungsmittel
2×

Versuchsvorschrift

A solution of 5.71 g of 6-hydroxymethyl-3,4-dihydro-2H-pyran in 100 ml of dimethylformamide was added dropwise, whilst ice-cooling, to a mixture of 2.18 g of a 55% w/w suspension of sodium hydride in mineral oil and 100 ml of dimethylformamide. The mixture was stirred at room temperature for 60 minutes, after which 6.33 g of benzyl chloride were added. The reaction mixture was stirred for 16 hours, and then poured into 1 liter of water and extracted twice with ethyl acetate. The extract was washed with water, dried and condensed by evaporation under reduced pressure. The oily residue, 13 g, was subjected to column chromatography through 200 g of silica gel. The fraction eluted with mixtures of diethyl ether and hexane ranging from 4:100 to 5:100 by volume gave 9.40 g of the title compound as a colorless oily substance, boiling at 125°-130° C. (bath temperature)/1 mmHg (133 Pa).

Aufarbeitung

  1. stirringThe reaction mixture was stirred for 16 hours
  2. extractionextracted twice with ethyl acetate
  3. washThe extract was washed with water
  4. customdried
  5. customcondensed
  6. customby evaporation under reduced pressure
  7. washThe fraction eluted with mixtures of diethyl ether and hexane ranging from 4:100 to 5:100 by volume

Quellen und Nachweise

ORD-Eintrag
ord-265b1d52489e420a829c2783c2dcc1ac
Quelldatensatz
uspto-grants-1988_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04794183

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