HuagongsheHuagongshe Chemistry Print Report · For research reference only
2',4'-Dihydroxyacetophenone → HCID 67245703, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2',4'-Dihydroxyacetophenone | HCID 6990 | — |
| Reactant | Benzyl bromoacetate | HCID 62576 | — |
| Product | HCID 67245703 | HCID 67245703 | — |
Reaction Steps
1-(2,4-Dihydroxy-phenyl)-ethanone was treated with 1 equivalent of benzyl 2-bromoacetate and processed as described in the synthesis of example 20a to obtain the title compound. The crude was purified using flash chromatography (silica gel, 3% CH3CN in chloroform) and crystallization was effected using ether-PE 60-80° C. Yield, 75%, white solid; mp, 66-67° C.; MS (EI): 300 (M+), 285, 165, 91 (100%); analysis: C17H16O5 requires C, 67.99; H, 5.37; found: C, 67.99; H, 5.53%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07759387B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-adaabce8919345f78dbaccc9b9c36dd1 |
| Source note | uspto-grants-2010_07 |