Diethyl Ether → HCID 23677780, compound
Reaction equation
[CH3:1][O-].[Na+:3].[CH3:4][O:5][CH:6]=[O:7].CC[O:10][CH2:11][CH3:12]>>[O:7]=[C:6]1[O:5][CH2:4][CH2:1]/[C:12]/1=[CH:11]/[O-:10].[Na+:3]Participants
4
Procedure
To a cooled suspension of 54.0 g. (1 mole) of sodium methoxide in a liter of dry ether, a mixture of 80 ml. (1.3 moles) of methylformate and 76 ml. (1 mole) of y-butyrolactone was added dropwise with stirring over a 2-h period. The stirring was continued at room temperature overnight. The reaction mixture was then cooled in an ice bath for 1 hr. to complete the separation of the cream-colored product which was then collected, washed with dry ether, and dried under vacuum to yield sodium (Z)-(2-oxodihydrofuran-3(2H)-ylidene)methanolate (123 g, 90%)
Workup
- additionTo a cooled suspension of 54.0 g
- temperatureThe reaction mixture was then cooled in an ice bath for 1 hr
- customthe separation of the cream-colored product which
- customwas then collected
- washwashed with dry ether
- customdried under vacuum
Sources & evidence
- ORD record
- ord-833a8a94f03e4faeaa5874fd0f1df08f
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09422271B2
Reaction notes
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