HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976605Generated: October 29, 2026
2'-Bromoacetophenone → HCID 21468921, compound
https://huagongshe.com/reaction/976605
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2'-Bromoacetophenone | HCID 75060 | — |
| Reactant | 1,1-Bis(methylthio)-2-nitroethylene | HCID 83623 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Gold's Reagent | HCID 11008255 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21468921 | HCID 21468921 | 11.9% |
Reaction Steps
2'-Bromoacetophenone(0.1 moles, 20.0 g) was reacted with sodium mothoxide (0.13 moles) in 150 ml methanol and treated with Gold's Reagent (0.13 moles, 21.2 g) according to the procedure in J. Org, Chem, 45: 4525 (1988). The intermediate was purified by chromatography over silica gel eluted with 75-100% ethyl acetate in hexane. The resulting amine was dissolved in ethanol with 1,1-bis(methylthio)-2-nitroethylene (0.074 moles, 12.3 g) and sodium acetate (22.5 g) and refluxed for two hours. An additional 45 g of sodium acetate was added. The solution continued to reflux for 16 hours. The reaction was concentrated. Ethyl acetate and water were added. The organic phase was dried and evaporated. The product was chromatographed over silica gel eluted with a gradient of 25-100% ethyl acetate in hexane to yield 2.6 g of 2-amino-6-(2-bromophenyl)-3-nitropyridine. (MS)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05612360 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-987a00a6cbef4c0abba998f06425ab82 |
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| Source note | uspto-grants-1997_03 |
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