Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Isoleucine | HCID 6306 | — |
| Reactant | Bis(4-nitrophenyl) carbonate | HCID 78756 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67520545 | HCID 67520545 | 28% |
Reaction Steps
A 300 ml round-bottomed flask equipped with a Dimroth condenser was charged with 13.13 g (100 mmol) of L-isoleucine and 1000 ml of tetrahydrofuran. After the addition of 30.4 g (100 mmol) of bis(4-nitrophenyl) carbonate, the mixture was stirred at 60° C. for 20 hours. After evaporating the solvent, the residue was purified by column chromatography to obtain 8.3 g of N-(4-nitrophenoxycarbonyl)-L-isoleucine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178641B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-ee8f210c7ecb4d07a1f8572af3dfdc4c |
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| Source note | uspto-grants-2012_05 |
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