Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 8-(Dimethylamino)-1,4-dioxaspiro[4.5]decane-8-carbonitrile | HCID 360977 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | HCID 178418336 | HCID 178418336 | — |
| Product | HCID 21093242 | HCID 21093242 | — |
Reaction Steps
50 g 8-dimethylamino-1,4-dioxaspiro[4.5]decane-8-carbonitrile were dissolved in 400 ml analytical grade tetrahydrofuran, 214 ml 2.0 molar benzylmagnesium chloride solution in THF were added under a nitrogen atmosphere and the mixture was stirred overnight at room temperature. For working up, 200 ml saturated ammonium chloride solution were added, while cooling with ice, the phases were separated, the aqueous phase was extracted twice with 250 ml diethyl ether each time, the combined organic phases were dried over sodium sulfate, filtered and concentrated and the residue was largely freed from solvent residues in vacuo. The crude (8-benzyl-1,4-dioxaspiro[4.5]dec-8-yl)-dimethylamine obtained (78.4 g) was stirred, without further purification, with a mixture of 200 ml conc. hydrochloric acid (32 per cent by weight) and 120 ml water for 24 hours at room temperature. The reaction mixture was then first washed three times with 100 ml diethyl ether each time, then rendered alkaline by addition of sodium hydroxide solution (32 per cent by weight), while cooling with ice, and extracted three times with 100 ml methylene chloride each time, the combined methylene chloride extracts were dried over sodium sulfate, filtered and concentrated and the residue was largely freed from solvent residues in vacuo. 50.4 g 4-benzyl-4-dimethylaminocyclohexanone were obtained as a brownish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07678834B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-50f88c392c6b4ce29e2042292dc9b784 |
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| Source note | uspto-grants-2010_03 |
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