Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 22723482 | HCID 22723482 | — |
| Reactant | HCID 86734362 | HCID 86734362 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54325626 | HCID 54325626 | — |
Reaction Steps
2g of 2-phenyl-3-(4-bromophenyl)-3-chloro-acrylaldoxime (5.9 m moles) were suspended in 50 ml of THF. The mixture was cooled to 0° C and, successively, 5 ml of sodium hydroxide solution and 1.14 g of p-toluene-sulfochloride were added. The mixture was stirred for 1 hour at 10° C and evaporated at room temperature. The solid residue was taken up with a small amount of methylene chloride and applied onto a column with basic aluminum oxide in n-hexane. Elution was effected with petroleum ether and then with methylene chloride. In this way pure 2-phenyl-3-(4-bromophenyl)-3-chloro-acrylonitrile (melting point: 128° -130° C) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04001431 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-9f8c51ed10c246458dfd37e4ceeeec64 |
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| Source note | uspto-grants-1977_01 |
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