Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 2-Piperidone | HCID 12665 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2-Morpholinoaniline | HCID 735756 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 178420463 | HCID 178420463 | — |
Reaction Steps
A solution of delta-valerolactam (24 g) in dry benzene (100 ml) was cooled to 10° C. in ice-water and treated with freshly distilled phosphorus oxychloride (22.2 ml) under nitrogen over a period of 10-15 minutes. The initial white solid formed changed to a clear yellow oil over 3 hours. A solution of 4-(2-aminophenyl)morpholine (36 g) in dry benzene (150 ml) was added and the mixture heated at 65° C. with stirring for 32 hours. The benzene layer was decanted, the oil washed twice with benzene (2×40 ml), ether (100 ml) was added and the mixture cooled in ice treated with 10% aqueous sodium hydroxide solution to alkaline pH, with stirring. The aqueous layer was extracted with ether (2×100 ml) and the combined ether extracts washed with water, brine and dried. The solution was filtered and the solvent removed to give a thick oil which solidified on trituration with hexane. The crude solid was crystallised from hot hexane to yield 4-[ 2-(2-piperidinylideneamino)phenyl]morpholine (m.p. 89°-90° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05373008 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-da4fdda5a5e34fc0819f4787ac178f1d |
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| Source note | uspto-grants-1994_12 |
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