HuagongsheHuagongshe Chemistry Print Report · For research reference only
Beta-Alanine → HCID 86733766, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Beta-Alanine | HCID 239 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Bromopropanoyl chloride | HCID 97980 | — |
| Reactant | HCID 178526132 | HCID 178526132 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 86733766 | HCID 86733766 | — |
Reaction Steps
8.9g (0.10 mol) of β-alanine was dissolved in 100 ml of water. To the solution was added 20 ml of triethylamine and then was added dropwise 22.2g (0.13 mol) of 2-bromopropionylchloride over one hour while stirring and ice-cooling. The mixture was stirred for a further 2 hours. To the mixture was added the filtrate which had been prepared by neutralizing 19.5g (0.14 mol) of thiobenzoic acid with an aqueous KOH and filtering the solution, followed by stirring overnight. Crystals precipitated were recovered by filtration, washed with water and dried to give 20.8g of N-(2-benzoylmercaptopropionyl-β-alanine. After recrystallization from benzene, the product had a melting point of 94° - 97°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03971828 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-be8c00eb578840998e24f8c318c3868f |
| Source note | uspto-grants-1976_07 |