HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → Carboxyphenylmethyl 5-amino-4-oxopentanoate hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | t-butyl alpha-[5-(Boc-amino)-4-oxopentanoyloxy]-phenylacetate | HCID 90034569 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Carboxyphenylmethyl 5-amino-4-oxopentanoate hydrobromide | HCID 90034508 | 71% |
Reaction Steps
This compound was prepared from the product of 6b (2.75 g; 6.5 mmol) and 33% HBr in acetic acid (5 mL) as described in Example 1c. The crude product was purified by flash chromatography on a 40×55 mm silica gel 60 column eluted with 10% methanol in acetonitrile (400 mL) collecting 20×10 ml fractions. After evaporation of fractions 4-15 and vacuum-drying for 48 h at 40° C. and 0.01 mm Hg 1.60 g (71%) product was obtained (orange foam, mp 77-80° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09249086B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-0051722436894c909e7660be6e1f4f55 |
| Source note | uspto-grants-2016_02 |