HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → Butanoic acid, 4-bromo-2-(methoxyimino)-3-oxo-, ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Ethyl (2Z)-2-methoxyimino-3-oxo-butanoate | HCID 43493 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Butanoic acid, 4-bromo-2-(methoxyimino)-3-oxo-, ethyl ester | HCID 54053279 | — |
Reaction Steps
Bromine (100 g.) was dropwise added over 40 minutes under reflux to a solution of ethyl 2-methoxyiminoacetoacetate (a mixture of syn and anti isomers) (100 g.) in a mixture of carbon tetrachloride (300 ml.) and acetic acid (300 ml.). The mixture was stirred at 70° to 80° C. until the evolution of hydrogen bromide ceased. The reaction mixture was washed twice with water (300 ml.), a sodium bicarbonate aqueous solution and a saturated sodium chloride aqueous solution and dried over magnesium sulfate. The solution was treated with activated charcoal (2 g.) and concentrated under reduced pressure to give ethyl 2-methoxyimino-4-bromoacetoacetate (a mixture of syn and anti isomers) (120.8 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04166115 |
| Source dataset | uspto-grants-1979_08 |
| ORD ID | ord-207f3892e14f4f30b0ca214fd23a7b11 |
| Source note | uspto-grants-1979_08 |