Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Bromide ion | HCID 259 | — |
| Edukt | Hydrogen Peroxide | HCID 784 | — |
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Chloroselenobenzene | HCID 21928 | — |
| Edukt | Benzenesulfinyl chloride | HCID 4190003 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Perbenzoic acid | HCID 523077 | — |
Reaktionsschritte
The diene (2) of step (B) is treated with a halogenating agent such as phenylselenyl chloride or bromide or phenylsulfinyl chloride, preferably phenylselenyl chloride, in an approximately equimolar ratio in an inert solvent at about -80° C., for approximately 20 minutes; illustrative of such inert solvents are methylene chloride, ether and the like. After a standard workup the product residue is dissolved in an ethereal solvent, chilled to about 0° C. and oxidized with an agent such as 30% hydrogen peroxide or a peroxy acid such as peroxybenzoic acid to yield a halohydrin analog (3).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04894466 |
|---|
| Quelldatensatz | uspto-grants-1990_01 |
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| ORD ID | ord-87cf1d353afc46b09fcef30e59489fe9 |
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| Quellennotiz | uspto-grants-1990_01 |
|---|