Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | HCID 66703997 | HCID 66703997 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66704009 | HCID 66704009 | 58% |
Reaction Steps
tert-Butyl (2S)-2-(4-(3-bromopropyloxy)phenyl)morpholine-4-carboxylate (2.0 g, 5.0 mmol) was added to a solution of sodium hydride (60% in oil, 0.22 g, 5.50 mmol) and pyrrolidine (0.43 g, 6.05 mmol) in tetrahydrofuran (40 ml) at room temperature and the mixture was stirred at 80° C. for 5 hours. The mixture was partitioned between water and chloroform. The organic layer was washed with brine, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting 5-10% methanol in chloroform to furnish tert-butyl (2S)-2-(4-(3-(pyrrolidin-1-yl)propyloxy)phenyl)morpholine-4-carboxylate (1.13 g, 58%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106045B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-b089b24c641449d19e251ab70f9b1ef6 |
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| Source note | uspto-grants-2012_01 |
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