Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 57931197 | HCID 57931197 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 57931190 | HCID 57931190 | — |
Reaction Steps
To a solution of lithium aluminium hydride in diethyl ether (1 M, 1.6 mL) at −78° C. was added a solution of 1′-(propylsulfonyl)-1,4′-bipiperidine-4′-carbonitrile (0.40 g, 1.34 mmol) in diethyl ether (10 mL) over 30 min. The mixture was stirred cold for 1 h then allowed to warm to room temperature and stirred for 2 h. The resultant mixture was cooled in an ice-bath and to the mixture was added water (0.17 mL), 15% NaOH solution (0.17 mL) then water (0.17 mL). The resultant white granular solid was filtered off and the filter-cake rinsed twice with diethyl ether. The filtrate was evaporated to give {[1′-(propylsulfonyl)-1,4′-bipiperidin-4′-yl]methyl}amine as a clear oil which was used in the next step without further purification; m/z (ES+) 304 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07947714B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-a45675908f4e4207bb36c4fd36301eb8 |
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| Source note | uspto-grants-2011_05 |
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