HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Bromo-1-cyclohexyl-3-dimethylamino-propenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-Cyclohexyl-3-dimethylamino-propenone | HCID 11095241 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-1-cyclohexyl-3-dimethylamino-propenone | HCID 91622408 | 99.8% |
Reaction Steps
To an ice cold solution of 1.18 g (6.51 mmol) of 1-cyclohexyl-3-dimethylamino-propenone in 8 mL of dichloromethane was added dropwise 1.04 g (6.51 mmol) of bromine via an addition funnel. The reaction mixture was stirred at 0□C. for 0.5 h and then 0.9 mL (6.51 mmol) of triethylamine in 10 mL of ether was added dropwise. The mixture was stirred at 0□C. for 1 h and allowed to warm up to rt. A light yellow solid precipitated from the solution, and it was separated by filtration. The filtrate was then concentrated to give 1.69 g of 2-bromo-1-cyclohexyl-3-dimethylamino-propenone as a brown solid as indicated by 1H NMR. The product was used in the next reaction without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07449488B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-932a8e417ef5421dbb42200b879a9fef |
| Source note | uspto-grants-2008_11 |