Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 88428340 | HCID 88428340 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Product | HCID 57262022 | HCID 57262022 | — |
Reaction Steps
To a stirred suspension of crude amino acid salt (2S,3S)-2-amino-3-(methoxycarbonyl)pentanoic acid hydrobromide (19.6 g) of Example 7 in aqueous hydrobromic acid (2.5N), cooled to -9° C. with an ice water-salt-acetone bath, was added sodium nitrite (10.0 g, 144.9 mmol) in small portions over a 1.5 h period, keeping the internal temperature (measured by electronic internal temperature probe) below -7° C. The reaction mixture was stirred for 2 h in the cooling bath after the addition was complete, then it was extracted with ethyl acetate (2×500 mL). The combined organic layers were washed with saturated aqueous sodium chloride (2×250 mL), dried (MgSO4), and concentrated in vacuo to give the bromoacid which slowly solidified to a waxy solid (13.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05322942 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-1547a1983e9c48269eb0b46f13c24bc4 |
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| Source note | uspto-grants-1994_06 |
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