HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3-Buten-2-one, 3-bromo-4-ethoxy-1,1,1-trifluoro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Ethoxy-1,1,1-trifluoro-3-buten-2-one | HCID 2780395 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-Buten-2-one, 3-bromo-4-ethoxy-1,1,1-trifluoro- | HCID 3729078 | 78.5% |
Reaction Steps
9.8 g (0.055 mole) of N-bromosuccinimide and 100 mg azoisobutyronitrile are added to a solution of 8.4 g (0.05 mole) of 4-ethoxy-1,1,1-trifluoro-but-3-en-2-one in 50 ml of tetrachloromethane. The mixture is then refluxed for 8 hours, the cooled solution is filtered and the filtrate is concentrated. 13.4 g of a crude product are obtained whiose distillation under reduced pressure gives 9.7 g of 3-bromo-4-ethoxy-1,1,1-trifluorobut-3-en-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04876393 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-54d553944886458398a857e74ff03636 |
| Source note | uspto-grants-1989_10 |