Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isobutyl iodide | HCID 10556 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 15-Crown-5 | HCID 36336 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | HCID 91343849 | HCID 91343849 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69795369 | HCID 69795369 | — |
Reaction Steps
1 g of tert-butyl (3R,5S,6R)-3-allyl-2-oxo-5,6-diphenylmorpholine-4-carboxylate was dissolved in 20 ml of THF. 3 ml of 15-crown-5 were added, and the mixture was cooled to −78° C. Then 1.4 ml of a 2 M solution of NaHMDS in THF were added dropwise. The mixture was stirred for 10 min and then 300 μl of isobutyl iodide were added dropwise. The temperature was allowed to rise to 0° C. over the course of 6 h, and then the reaction was stopped by adding 50 ml of saturated ammonium chloride solution. The aqueous phase was extracted 3 times with 50 ml of ethyl acetate each time, and the combined organic phases were dried with MgSO4. The solvents were removed in vacuo and the residue was chromatographed on silica gel with heptane/ethyl acetate 10:1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07008957B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-3590330246b846f1bc74a138015384c8 |
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| Source note | uspto-grants-2006_03 |
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