HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl 2-bromo-3-hydroxybutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Ethyl trans-crotonate | HCID 429065 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 2-bromo-3-hydroxybutanoate | HCID 12541051 | — |
Reaction Steps
To a mixture of 10 g of ethyl crotonate, 40 ml of dioxane and 60 ml of water, at 0°, is slowly added 15 g of N-bromosuccinimide. After addition is complete, the reaction is allowed to stand at RT for 17 hr with stirring. The reaction is taken up in ether, washed with water and saturated sodium sulfite, dried over magnesium sulfate and evaporated under reduced pressure to yield ethyl 2-bromo-3-hydroxybutanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04411912 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-4c31462e90ea477cb145a34ca79e7872 |
| Source note | uspto-grants-1983_10 |