Water → 2H-Pyran, 3,4-dihydro-6-[(phenylmethoxy)methyl]-
Reaction equation
[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]=1Participants
Procedure
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).
Workup
- stirringThe reaction mixture was stirred for 16 hours
- extractionextracted twice with ethyl acetate
- washThe extract was washed with water
- customdried
- customcondensed
- customby evaporation under reduced pressure
- washThe fraction eluted with mixtures of diethyl ether and hexane ranging from 4:100 to 5:100 by volume
Sources & evidence
- ORD record
- ord-265b1d52489e420a829c2783c2dcc1ac
- Source dataset
- uspto-grants-1988_12
- Patent number
- US04794183
Reaction notes
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