HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aminoisobutyric acid → HCID 21829923, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aminoisobutyric acid | HCID 6119 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Bromophenylacetyl chloride | HCID 598182 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 21829923 | HCID 21829923 | 55.6% |
Reaction Steps
Ammonium hydroxide (1.6 g) aqueous solution (40 mL) was added to aminoisobutyric acid (2.1 g). The solution was cooled to 0° C., to which a solution of a-bromophenylacetyl chloride (6 g) in acetonitrile (5 mL) was slowly added dropwise. After the addition was completed, the mixture was warmed to room temperature and stirred overnight. The precipitate was filtered off and washed with water to give 3.4 g of 2-(α-bromophenylacetylamino)isobutyric acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05977027 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-3a561411841846b79be8d7d6baf0c5f6 |
| Source note | uspto-grants-1999_11 |