HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → HCID 21435299, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | 4-Propylphenol | HCID 12580 | — |
| Reactant | 4-(Trifluoromethyl)phenol | HCID 67874 | — |
| Product | HCID 21435299 | HCID 21435299 | — |
| Product | HCID 21510500 | HCID 21510500 | — |
Reaction Steps
When 4-n-propylphenol or 4-trifluoromethylphenol is reacted with α-bromoacetophenone according to the procedure described in Example 14 and the resulting product is cyclized by heating with polyphosphoric acid at 80° as described therein, 3-phenyl-5-n-propylbenzofuran and 3-phenyl-5-trifluoromethylbenzofuran are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03983245 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-627c8f42df41435186875b1282d295ec |
| Source note | uspto-grants-1976_09 |