Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ethane, 1,2-dibromo-1-ethoxy- | HCID 102915 | — |
| Reactant | HCID 178418682 | HCID 178418682 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Bromo-2-ethoxyhexane | HCID 12560781 | — |
Reaction Steps
To a stirred solution of 1.68 moles of n-butylmagnesium bromide, as a 1.7 M solution in ether, is added dropwise a solution of 300 g. of 1,2-dibromo-2-ethoxyethane in 750 ml. of ether during a period of 2 hours at -15° C. The resulting mixture is stirred for one hour while warming to 20° C., then cooled to 0° C., and treated while stirring with 500 ml. of water, followed by 100 ml. of 4 N hydrochloric acid. The organic layer is washed with brine, dried over magnesium sulfate and concentrated. The residue is distilled to provide a colorless liquid, b.p. 83°-84° C., 18 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04404393 |
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| Source dataset | uspto-grants-1983_09 |
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| ORD ID | ord-9bb8cb5db8f943f896de7128be13c121 |
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| Source note | uspto-grants-1983_09 |
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