HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromophenol → HCID 21447344, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromophenol | HCID 7244 | — |
| Reactant | HCID 70637816 | HCID 70637816 | — |
| Product | HCID 21447344 | HCID 21447344 | — |
Reaction Steps
Starting with 2-bromophenol and alpha-bromo-3,4-dichloroacetophenone and using Process A as described in Examples 1 and 2, the compound 7-bromo-3-(3,4-dichlorophenyl)benzofuran is prepared. Using Process F as described in Examples 6 to 9, this compound is converted to 3-(3,4-dichlorophenyl)-7-benzofuranacetic acid, m.p. 158.5°-160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04013692 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-904e0643e71e436980f4388f1fc3bc01 |
| Source note | uspto-grants-1977_03 |