HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460701Generated: October 25, 2026
Triethylamine → 2-Bromo-1-cyclohexyl-3-dimethylamino-propenone
https://huagongshe.com/reaction/460701
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 |
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| Patent number | US07196111B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-8fe01bfc8ea44ddb88271c063a992a98 |
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| Source note | uspto-grants-2007_03 |
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