Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Chloroselenobenzene | HCID 21928 | — |
| Reactant | Benzenesulfinyl chloride | HCID 4190003 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Perbenzoic acid | HCID 523077 | — |
Reaction Steps
The diene (2) 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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05001241 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-942983f84d7b44448d9c69f330398bc7 |
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| Source note | uspto-grants-1991_03 |
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