Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 2R-(t-Boc)amino-1,4-dichloro-3S-hydroxybutane | HCID 11368909 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 88230374 | HCID 88230374 | 99.4% |
Reaction Steps
To a stirred solution of 2(R)-(t-butyloxycarbonyl)amino-1,4-dichloro-3(S)-hydroxybutane (100.0 mg, 0.389 mmol) in dry DMF (2.5 mL) were added imidazole (79.4 mg, 1.67 mmol), DMAP (4.8 mg, 0.039 mmol) and TBS-Cl (175.9 mg, 1.167 mmol) at room temperature under N2. The resulting solution was stirred at 50° C. for 12 h. The reaction mixture was diluted with EtOAc (30 mL), washed with 0.1 N citric acid solution (5 mL), sat aqueous NaHCO3 (5 mL), water (5 mL) and brine (5 mL), dried over anhydrous magnesium sulfate, filtered, concentrated and column-chromatographed (10% EtOAc in n-Hex) to provide 2(S)-t-butyldimetylsilyloxy-3(R))-(t-butyloxycarbonyl)amino-1,4-dichlorobutane as a colorless solid (144.6 mg)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06573388B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-0980e191f96c40d78480699f635c26ef |
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| Source note | uspto-grants-2003_06 |
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