HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → t-butyl alpha-[5-(Boc-amino)-4-oxopentanoyloxy]-phenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tert-butyl 2-bromo-2-phenylacetate | HCID 11000147 | — |
| Reactant | 5-((tert-Butoxycarbonyl)amino)-4-oxopentanoic acid | HCID 17989820 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | t-butyl alpha-[5-(Boc-amino)-4-oxopentanoyloxy]-phenylacetate | HCID 90034569 | 78% |
Reaction Steps
This compound was prepared from 5-(Boc-amino)-4-oxopentanoic acid (1.97 g; 8.5 mmol), the product of 6a (2.35 g; 8.7 mmol), and triethylamine (0.88 g; 8.7 mmol) in ethyl acetate (30 mL) as described in Example 1a. The crude product was purified by flash chromatography on a 65×55 mm silica gel 60 column eluted with ethyl acetate-hexane (1:2) (1100 mL) collecting 18×50 mL fractions. After evaporation of fractions 3-8, 2.79 g (78%) product was obtained (amber oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09249086B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-04cef073c8344c4382c5d0542e83d501 |
| Source note | uspto-grants-2016_02 |