Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 59243637 | HCID 59243637 | — |
| Solvent | AcOH THF water | HCID 21877175 | — |
| Product | HCID 59243586 | HCID 59243586 | — |
Reaction Steps
Cyclopentyl N-(tert-butoxycarbonyl)-O-[tert-butyl(dimethyl)silyl]-D-homoserinate (1.57 g, 3.9 mmol) was dissolved in acetic acid:THF:water (3:1:1, 100 ml). The reaction mixture was stirred at 30° C. for 16 hours for complete reaction. Ethyl acetate (200 ml) was added and washed with 1M Na2CO3, 1M HCl and brine. The ethyl acetate extracts were dried over magnesium sulphate and evaporated under reduced pressure to give the product as a clear oil which crystallised on standing (1.0 g, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106091B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-c614dae18db1483e8af32b9ba0c155c9 |
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| Source note | uspto-grants-2012_01 |
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