HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → Ethyl [6,7-dichloro-1-oxo-2-(p-chlorophenyl)-5-indanyloxy]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | 6,7-Dichloro-5-hydroxy-2-(p-chlorophenyl)-1-indanone | HCID 13065297 | — |
| Product | Ethyl [6,7-dichloro-1-oxo-2-(p-chlorophenyl)-5-indanyloxy]acetate | HCID 12774097 | — |
Reaction Steps
Reaction of of 6,7-dichloro-5-hydroxy-2-(p-chlorophenyl)-1-indanone with ethyl bromoacetate according to the procedure of Example 1, STEP (a), affords the title compound, m.p. 159.5°-160° (crystallized from ethanol-acetone).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04334088 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-a9990990ce474d7496b0dc59e992fedf |
| Source note | uspto-grants-1982_06 |