HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867091Generated: October 30, 2026
N-bromobutanimide → HCID 54087782, compound
https://huagongshe.com/reaction/867091
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 54471371 | HCID 54471371 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 54087782 | HCID 54087782 | — |
Reaction Steps
A mixture of 7.0 g (0.024 mol) of 1-(4-bromophenyl)-1-(3-pyridyl)-propene and 4.6 g (0.024 mol) of N-bromosuccinimide in 600 ml of carbontetrachloride was heated with stirring to 80° C. Then 0.5 g. of α,α-azabisbutyronitrile was added as radical initiator and the mixture was refluxed for 2 hours. After cooling to ambient temperature, the reaction mixture was filtered and the filtrate was evaporated in vacuo to 100 ml. NMR on the residual solution indicated a 1:1-mixture of the E- and Z-3-(4-bromophenyl)-3-(3-pyridyl)allylbromides. This solution was used directly in the preparation of the end product without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04102887 |
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| Source dataset | uspto-grants-1978_07 |
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| ORD ID | ord-30f324fc0a774d4c92d5202715781a2e |
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| Source note | uspto-grants-1978_07 |
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