Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | N-Cbz-D-Asparagine | HCID 1712147 | — |
| Reactant | Iodo benzene diacetate | HCID 12217721 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Z-D-Dap-OH | HCID 6950592 | — |
Reaction Steps
To a stirred solution of iodobenzene diacetate (7.26 g) in a mixture of ethyl acetate (44 ml), acetonitrile (44 ml) and water (22 ml) was added 2(R)-benzyloxycarbonylamino-succinamic acid (5.0 g) at ambient temperature. After stirred for 3 hours, the reaction mixture was cooled to 5° C., followed by stirring for 2 hours. Insoluble material was collected by filtration, washed with ethyl acetate, and dried under reduced pressure to give 2(R)-benzyloxycarbonylamino-β-alanine (4.15 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06538007B1 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-caef429ac5654e6cb5b66ed43a41e2bd |
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| Source note | uspto-grants-2003_03 |
|---|