Diethyl Ether → HCID 23677780, compound

HRID 1484947Notes

Reaction equation

HRID 1484947 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

  1. additionTo a cooled suspension of 54.0 g
  2. temperatureThe reaction mixture was then cooled in an ice bath for 1 hr
  3. customthe separation of the cream-colored product which
  4. customwas then collected
  5. washwashed with dry ether
  6. customdried under vacuum

Sources & evidence

ORD record
ord-833a8a94f03e4faeaa5874fd0f1df08f
Source dataset
uspto-grants-2016_08
Patent number
US09422271B2

Reaction notes

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