Sodium Methoxide → HCID 86734594, compound
Reaction equation
[CH3:1][O:2][C:3]([N:15]=[C:16]=[O:17])=[CH:4][C:5]1[CH:10]=[CH:9][C:8]([O:11]C(=O)C)=[CH:7][CH:6]=1.C[O-].[Na+]>CO>[CH3:1][O:2][C:3]([N:15]=[C:16]=[O:17])=[CH:4][C:5]1[CH:10]=[CH:9][C:8]([OH:11])=[CH:7][CH:6]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 50 °C
Procedure
A suspension of 23.5 g (0.1 mol) of p-(2-methoxy-carbonylaminovinyl)-acetoxybenzene in 300 ml of absolute methanol, which is mixed with a solution of 5.4 g of sodium methoxide in 30 ml of methanol, is warmed to 50° C for 15 minutes. Thereafter the mixture is evaporated to dryness under reduced pressure. The resulting crude sodium salt of [2-methoxy-carbonylaminovinyl]-phenol is dissolved in 100 ml of water, 50 ml of 2 N hydrochloric acid are added to the solution and the phenol which has separated out is extracted with ethyl acetate. The organic phase is washed with water, dried over sodium sulphate and evaporated in vacuo. Crude p-(2-methoxy-carbonylaminovinyl)-phenol is obtained as an oil. This can be used, as shown below, without further purification. A sample crystallised from ether showed a melting point of 169°-170° C.
Workup
- customThereafter the mixture is evaporated to dryness under reduced pressure
- dissolutionThe resulting crude sodium salt of [2-methoxy-carbonylaminovinyl]-phenol is dissolved in 100 ml of water
- addition50 ml of 2 N hydrochloric acid are added to the solution
- customthe phenol which has separated out
- extractionis extracted with ethyl acetate
- washThe organic phase is washed with water
- dry with materialdried over sodium sulphate
- customevaporated in vacuo
Sources & evidence
- ORD record
- ord-51c07f65fa17402fb1a2fe76604ce5de
- Source dataset
- uspto-grants-1977_03
- Patent number
- US04014920
Reaction notes
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