HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexanoyl bromide → 2-Amino-3-methylpentanoic hexanoic anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexanoyl bromide | HCID 13226800 | — |
| Reactant | Sodium 2-amino-3-methylpentanoate | HCID 23662724 | — |
| Product | 2-Amino-3-methylpentanoic hexanoic anhydride | HCID 25006169 | — |
Reaction Steps
Finally, in a dry 2-necked, round bottomed flask, fixed with a separatory funnel, containing 10.81 g (60 mmol) of the prepared hexanoyl bromide, and side arm water condenser fixed with a dry receiving flask, is placed 11.03 g (72 mmol) of sodium 2-amino-3-methylpentanoate. The round bottomed flask is placed in an ice bath and the hexanoyl bromide is added drop wise. After addition is completed the mixture is shaken and the ice bath is replaced by a heating mantle. The flask is then heated until no more solution is dropping into the receiving flask. This crude distillate is then further fractionally distilled to yield 2-amino-3-methylpentanoic hexanoic anhydride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07511162B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-06008332fead487594dfab2b7e8eb607 |
| Source note | uspto-grants-2009_03 |