HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → Ethyl 2-(2-formamido-5-bromothiazol-4-yl)-2-methoxyiminoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Ethyl 2-(2-formamidothiazol-4-yl)-2-methoxyiminoacetate | HCID 53737196 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Ethyl 2-(2-formamido-5-bromothiazol-4-yl)-2-methoxyiminoacetate | HCID 53894989 | 94.3% |
Reaction Steps
A small amount of benzoyl peroxide was added to a suspension of ethyl 2(2-formamidothiazol-4-yl)-2-methoxyiminoacetate (syn isomer, 7.55 g.) and N-bromosuccinimide (5.75 g.) in dry benzene (150 ml.) and refluxed under heating for an hour. After cooling, the reaction mixture was washed with water three times, dried over magnesium sulfate, treated with activated charcoal and then evaporated in vacuo. The residue was pulverized with n-hexane, and the precipitates were collected by filtration, washed with n-hexane and water successively and dried to give ethyl 2-(2-formamido-5-bromothiazol-4-yl)-2-methoxyiminoacetate (syn isomer, 9.3 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04729991 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-92a1c6d0c83a42498cc3554908449f1e |
| Source note | uspto-grants-1988_03 |