Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Aminoisobutyric acid | HCID 6119 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Propanoyl bromide, 2-bromo- | HCID 79047 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 22253670 | HCID 22253670 | 70.9% |
Reaction Steps
A stirring mixture of 2-aminoisobutyric acid (52.08 g; 0.51 mol), sodium hydroxide (20.20 g; 0.51 mol), water (200 ml) and chloroform (50 ml) was cooled to −12° C. 2-Bromopropionyl bromide (100 g; 0.46 mol) in chloroform (150 ml) was added to the mixture over 15 minutes. The reaction mixture was then allowed to warm to room temperature after which time the mixture was filtered to isolate the solid that had precipitated. The solid was combined with hot toluene (700 ml) and this mixture was then allowed to cool. The while solid was isolated by filtration and was dried under vacuum to afford 77.60 g (70% yield) of 2-(2-bromopropionylamino)-2-methylpropionic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06680362B1 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-833e422a37d3473b93cdab7fb2f05a64 |
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| Source note | uspto-grants-2004_01 |
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