Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 68645089 | HCID 68645089 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178463965 | HCID 178463965 | — |
Reaction Steps
A 200 mL flask provided with a stirrer and a reflux condenser was charged in a nitrogen gas atmosphere with 1.2 g (0.05 mol) of metallic magnesium (cut form, 20-50 mesh size) (available from Yamaishi Metals Co., Ltd.), 20.0 g of tetrahydrofuran (available from Kanto Chemical Co., Inc.) and 0.3 g (0.003 mol) of ethyl bromide (available from Kanto Chemical Co., Inc.). The content was heated under reflux of solvent for 30 minutes. Then the reaction liquid was cooled to 5° C., and a solution in 30.0 g of tetrahydrofuran of 15.7 g (0.05 mol) of the p-(N-methyl-N-ethylaminohexyloxy)bromobenzene, synthesized at the above-mentioned step 2), was dropwise added at 5° C. over a period of 1 hour. The mixed reaction liquid was maintained at that temperature for 2 hours while being stirred. Thus a solution in tetrahydrofuran of the target p-(N-methyl-N-ethylaminohexyloxy)phenylmagnesium bromide was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07816475B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-c4a86ff0df274be9b3d3a4c1cf3081b9 |
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| Source note | uspto-grants-2010_10 |
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