HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 1-Bromo-4-chloro-3,3,6-trimethylhept-5-en-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4-Chloro-3,3,6-trimethylhept-5-en-2-one | HCID 13298322 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-Bromo-4-chloro-3,3,6-trimethylhept-5-en-2-one | HCID 20071053 | — |
Reaction Steps
6.03 g (0.032 mol) of 2,5,5-trimethyl-4-chloro-2-hepten-6-one are dissolved in 75 ml of chloroform, 2 drops of an ethereal hydrogen chloride solution are added, and 5.12 g (0.032 mol) of bromine are then added in one portion at 25° C. The mixture is stirred for 2.5 hours at room temperature, and hydrogen bromide and solvent are distilled off in vacuo; the final residues are removed in a high vacuum. 8.7 g are obtained of crude, 2,5,5-trimethyl-4-chloro-7-bromo-2-hepten-6-one, the structure of which is confirmed by the 1H-NMR spectrum. It is used directly in the next stage:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04992577 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-1813d1790b8a4796a8c9a3d3d6daf630 |
| Source note | uspto-grants-1991_02 |