HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Flutolanil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(Trifluoromethyl)benzoyl chloride | HCID 67561 | — |
| Reactant | 3-(Propan-2-yloxy)aniline | HCID 573220 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Flutolanil | HCID 47898 | 91% |
Reaction Steps
To a tetrahydrofuran solution containing 1.5 g (0.01 mole) of m-isopropoxyaniline and 1.2 g (0.011 mole) of triethylamine, while being cooled in ice water, was added slowly 2.3 g (0.011 mole) of o-trifluoromethylbenzoyl chloride. After having been stirred for 2 hours at room temperature, the reaction mixture was freed from triethylamine hydrochloride by filtration and then from the solvent by distillation under reduced pressure. The residue was recrystallized from n-hexane to obtain 2.9 g (91% yield) of the intended product melting at 95° to 97° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04093743 |
| Source dataset | uspto-grants-1978_06 |
| ORD ID | ord-4f116d2198b148e8ad29c69f17b767cf |
| Source note | uspto-grants-1978_06 |