Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 54088444 | HCID 54088444 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12043747 | HCID 12043747 | 52% |
Reaction Steps
10 ml of water was added to 2.00 g (8.57 mmol) of (R)-4-t-butoxycarbonylamino-3-hydroxybutanohydrazide (optical purity: >99.9%e.e.), and the mixture was cooled to 0° C. A 0.89 g (8.57 mmol) of 35% HCl was added thereto dropwise over 10 min, and then an aqueous solution of 0.59 g (8.57 mmol) of sodium nitrite dissolved in 2.0 ml of water was further added thereto dropwise slowly. After the reaction mixture was stirred for 1 hour at that temperature, the thus prepared reaction mixture was added to 10 ml of warm water (50° C.) dropwise over 1 hour. After the addition, the mixture was further stirred for 1 hour, cooled to room temperature, and then extracted thrice with a 20 ml portion of ethyl acetate. The extracted ethyl acetate was then concentrated to give 1.06 g of a crude product. The crude product was subjected to column chromatography (ethyl acetate) to obtain 0.96 g (52%) of the title compound. Melting point: 115.5° C. Optical purity: >99.9%e.e.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06403804B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-70e06e2664834894b796bc7b15acdc32 |
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| Source note | uspto-grants-2002_06 |
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