HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl formate → Sodium (E)-2-cyano-2-[(methoxycarbonyl)(methyl)amino]ethenolate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Methyl cyanomethyl(methyl)carbamate | HCID 45087346 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Sodium (E)-2-cyano-2-[(methoxycarbonyl)(methyl)amino]ethenolate | HCID 57469797 | — |
Reaction Steps
0.46 g (0.01 mmol) of sodium methoxide is added under argon to tetrahydrofuran (solution A). Then 1.00 g (0.01 mmol) of methyl cyanomethyl(methyl)carbamate from Example 9A is added to 1.73 g (0.02 mmol) of ethyl formate. Solution A is slowly added dropwise to this mixture. The mixture is stirred at RT overnight. The solvent is concentrated in vacuo in a rotary evaporator, and diethyl ether is added to the residue. The crystals which have separated out are filtered off with suction and dried under high vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07173037B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-78a196e817e64eb8ab1ec95dfae2af59 |
| Source note | uspto-grants-2007_02 |