HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methyl 3-ethoxy-2-(ethoxyimino)-3-iminopropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Fluoride Ion | HCID 28179 | — |
| Reactant | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| Reactant | Methyl 3-amino-2-(ethoxyimino)-3-oxopropanoate | HCID 53690437 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-ethoxy-2-(ethoxyimino)-3-iminopropanoate | HCID 53663360 | — |
Reaction Steps
To a solution of Meerwein reagent (triethyloxonium tetrafluoroborate) {prepared from bron fluoride etherate (2.84 g) by a method of Org. Syn., 46, 113 (1966)} in methylene chloride (30 ml) was added methyl 2-carbamoyl-2-ethoxyiminoacetate (syn isomer, 2.6 g) and the mixture was stirred for 18 hours at room temperature. The reaction mixture was cooled in an ice-bath and triethylamine (3 g) was added thereto, followed by an addition of water (20 ml). The organic layer was separated out, dried over magnesium sulfate and evaporated to give crude methyl 3-imino-3-ethoxy-2-ethoxyiminopropionate (syn isomer) (5.0 g) as an oil. ##STR15##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04407798 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-c2c14045175f4522914e930aa28b5372 |
| Source note | uspto-grants-1983_10 |