Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | HCID 10401400 | HCID 10401400 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 23387582 | HCID 23387582 | 87% |
Reaction Steps
To a solution of N-BOC-L-isoleucine chloromethyl ester (19.6 g, 70 mmol) in acetonitrile (300 mL), was added sodium iodide (31.5 g, 210 mmol). The solution was stirred for 4 h at 60° C. The resulting suspension was filtered and the filtrate was evaporated. The residue was dissolved in CH2Cl2 and washed with aqueous sodium thiosulfate (0.1 M). The organic phase was dried (Na2SO4) and concentrated under reduced pressure. The crude product was column chromatographed (silica gel, 2% MeOH in CH2Cl2), to give 22.6 g of N-BOC-L-isoleucine iodomethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06974802B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-f635fd8c906c4a65bb9635b4ac8a3e55 |
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| Source note | uspto-grants-2005_12 |
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