HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704635Generated: November 2, 2026
Pyridine → alpha-Bromoacetyl-beta-diethylaminostyrene
https://huagongshe.com/reaction/1704635
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | Diethylstyrylamine | HCID 12773281 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | alpha-Bromoacetyl-beta-diethylaminostyrene | HCID 86736175 | — |
Reaction Steps
To a solution of 17.5 g. of diethylstyrylamine in 200 ml. of ether was added 8.5 g. of pyridine. The mixture was cooled to 5° C. and a solution of 20.1 g. of bromoacetyl bromide in 200 ml. of ether was added over a period of about 4 hours. The mixture was filtered and the residue on the filter was washed with 300 ml. of ether. The combined ether filtrate and washings was washed with 1 N hydrochloric acid, 0.1 N sodium hydroxide, saturated aqueous sodium chloride, and dried over magnesium sulfate and activated carbon. The mixture was filtered and the ether was evaporated to give a quantitative yield of α-bromoacetyl-β-diethylaminostyrene. The product was shown by NMR spectrum to be a mixture of the cis and trans isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04127581 |
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| Source dataset | uspto-grants-1978_11 |
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| ORD ID | ord-252d87e4efb34264971ba7c74e225d0d |
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| Source note | uspto-grants-1978_11 |
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