HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha-Hydroxyacetophenone → HCID 118093827, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha-Hydroxyacetophenone | HCID 68490 | — |
| Reactant | HCID 118093987 | HCID 118093987 | — |
| Product | HCID 118093827 | HCID 118093827 | — |
Reaction Steps
This compound was synthesized according to the procedure of Example 76, Step 5, using 4-bromo-2-nitro-3-phenoxyphenol and 2-hydroxy-1-phenylethanone as the starting materials. LCMS calculated for C20H15BrNO5 (M+H)+: m/z=428.0, 430.0. found: 427.9, 429.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09399640B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-c9281eaba1614e4aa9f414ab9927509b |
| Source note | uspto-grants-2016_07 |