Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromopropane | HCID 7840 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium Hydroxide | HCID 73981 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 20391526 | HCID 20391526 | — |
| Reactant | HCID 178455851 | HCID 178455851 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 57489118 | HCID 57489118 | — |
Reaction Steps
A solution of 11.0 g of 1-(o-fluorobenzyl)-2-(dimethylaminoacetyl)pyrrole, free base of Example 3a, in ether is added dropwise to a stirring solution of n-propylmagnesium bromide which is prepared from 1.67 g of magnesium turnings and 8.4 g of n-propylbromide. The mixture is refluxed for 4 hours, allowed to cool, hydrolized with ice-water and treated with concentrated ammonium chloride solution to dissolve the magnesium hydroxide precipitate. The organic phase is separated and the aqueous phase extracted with ether and the organic phases are combined, washed with a 5% sodium bicarbonate solution and water and dried. Removal of the ether leaves a crude yellow oil which is distilled at 133°-137° C./0.08 mm gives a light yellow oil of 1-(dimethylamino)-2-[1-(o-fluorobenzyl)-2-pyrryl]-2-hydroxypentane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04029672 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-58958dbd9b934d07a834afa8a752afc7 |
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| Source note | uspto-grants-1977_06 |
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