HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613197Generated: October 29, 2026
Hydrogen Bromide → HCID 9815549, compound
https://huagongshe.com/reaction/613197
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Carbobenzoxy-beta-alanyltaurine | HCID 9927496 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 9815549 | HCID 9815549 | 87.4% |
Reaction Steps
N-carbobenzoxy-β-alanyl-taurine (1.00 g, 3.4 mmol) was slurried in 23 ml glacial AcOH. To the mixture was added 3.4 mL HBr in AcOH (30 wt %) to result in a clear solution. The reaction was heated to 40° C. and allowed to mix overnight. The product precipitated out of solution and acetonitrile was added to force the precipitation. The mixture was filtered, the filter cake washed and the product collected. The crude Br salt was loaded onto an ion exchange column (Dowex AG1-XB8). The column was eluted with H2O. The product cut was collected and lyophilized to give 583 mg of β-alanyl-taurine (87.3%). The zinc salt was prepared by treatment with Zn(OH)2 in H2O, followed by lyophilization. (See FIG. 1 for reaction Scheme.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06007819 |
|---|
| Source dataset | uspto-grants-1999_12 |
|---|
| ORD ID | ord-0c43a9da23f445b8914c3a855bc66f21 |
|---|
| Source note | uspto-grants-1999_12 |
|---|