HuagongsheHuagongshe Chemistry Print Report · For research reference only
o-(Trifluoromethyl)benzaldehyde → HCID 88365257, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | o-(Trifluoromethyl)benzaldehyde | HCID 123067 | — |
| Reactant | HCID 21463257 | HCID 21463257 | — |
| Reactant | HCID 21463259 | HCID 21463259 | — |
| Product | HCID 88365257 | HCID 88365257 | — |
Reaction Steps
5-Chloro-2-hydroxy-2'-(trifluoromethyl)benzophenone [prepared from 2-bromo-4-chloro-(2-methyoxyethoxy)methoxybenzene and ortho-(trifluoromethyl)benzaldehyde as the starting materials: melting point, 71°-72° C. (recrystallized from hexane-isopropyl ether)] was reacted by a method similar to Process 1 of Reference Example 25 to yield 6-chloro-2-oxo-4-[2-(trifluoromethyl)phenyl)-2H-1-benzopyran-3-carboxylic acid ethyl ester as an oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05700810 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-71eb56b2e05b430ebc07e6fdbd31f843 |
| Source note | uspto-grants-1997_12 |