HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Acifluorfen-methyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | Methyl 2-nitro-5-[4-(trifluoromethyl)phenoxy]benzoate | HCID 13209694 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Acifluorfen-methyl | HCID 91642 | — |
Reaction Steps
Methyl 5-(4-trifluoromethylphenoxy)-2-nitrobenzoate is stirred with a catalytic amount of ferric chloride. The reaction mixture was heated to 70° C. under a continuous stream of chlorine gas. After 2.5 hours, the mixture was taken up in ether, shaken with water and the organic phase was dried over MgSO4. The ether was evaporated to afford methyl 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoate. NMR (CDCl3)δ8.2-7 (m,6) 4.0 (2,3). TLC (40% ether/hexane) Rf ≈.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04395570 |
| Source dataset | uspto-grants-1983_07 |
| ORD ID | ord-c85e0659d8554c0b9334c310b60f0b5a |
| Source note | uspto-grants-1983_07 |