Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Bromoacetic Acid | HCID 6227 | — |
| Reactant | HCID 23362653 | HCID 23362653 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86750085 | HCID 86750085 | — |
Reaction Steps
4-Hydroxy-2,6-piperidinedimethaneamine (10 mmol) is dissolved in water (10 ml). The pH is adjusted to 10 with 4M LiOH, and a solution of bromoacetic acid (55 mmol) and LiOH (55 mmol) in water (10 ml) is gradually added to the stirred mixture at ambient temperature. The temperature is gradually increased to 85° C. during 4 hours while the pH is kept in the alkaline range (8 to 10) with aqueous LiOH. The solution is allowed to cool to ambient temperature, neutralised with conc. hydrobromic acid, loaded on a strong cation exchanger (AG 5Wx4) and eluted with 6M aqueous ammonia. After evaporation down, the crude product is dissolved in water and lyophilised to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05587144 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-e69453459d3d4f188c1d23165312afa0 |
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| Source note | uspto-grants-1996_12 |
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