Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 2-Piperidinone, 3-methyl-1-(phenylmethyl)- | HCID 11106446 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10704698 | HCID 10704698 | — |
Reaction Steps
The reaction of 3-methyl-1-phenylmethyl-2-piperidinone (Meyers A I, Kunnen K B, Still W C (1987) "Conformational effects on the regiochemical metalation of C5-C13 N-benzyl lactams" J. Am. Chem. Soc., 109, 4405-4407.) (3.25 g, 16 mmol) with iodoethane (3.92 g, 25.1 mmol) in the presence of lithium diisopropylamide (prepared by treating diisopropylamine (2.42 g, 24 mmol) with butyllithium in hexanes (2.5 M, 9.2 mL, 22.9 mmol)) in THF (45 mL) and HMPA (2.4 ml,, 13.8 mmol) as described above in the preparation of Example 10, gave 5.90 g of pale yellow colored oil. Column chromatography over silica gel (hexanes-EtOAc, 9:1) afforded the product lactam (2.52 g, 68%) as a colorless viscous liquid. Analytical sample was prepared by bulb-to-bulb distillation (pot temp. 110-115° C. (1 mmHg)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06066666 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-e508cb9fd237467ab303f6f34331014d |
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| Source note | uspto-grants-2000_05 |
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