HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloro-5-(trifluoromethyl)benzaldehyde → 3-Bromo-5-(trifluoromethyl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloro-5-(trifluoromethyl)benzaldehyde | HCID 3857033 | — |
| Reactant | [3-Bromo-5-(trifluoromethyl)phenyl]methanol | HCID 29919767 | — |
| Product | 3-Bromo-5-(trifluoromethyl)benzaldehyde | HCID 16115438 | 85% |
Reaction Steps
The title compound was prepared from (3-bromo-5-(trifluoromethyl)phenyl)methanol (Reference Example 38) by a procedure similar to the one described for 3-chloro-5-(trifluoromethyl)benzaldehyde (Reference Example 31) to provide 3-bromo-5-(trifluoromethyl)benzaldehyde (22.03 g, 85%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853215B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-ffc1d73a0b334b76b5e93acbeae25e3f |
| Source note | uspto-grants-2014_10 |