Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | HCID 7732993 | HCID 7732993 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19367210 | HCID 19367210 | 145.1% |
Reaction Steps
A mixture of 102.4 g of 4-trifluoromethyl-2'-methoxybenzanilide prepared by the same manner as described in (1), 77.2 g of Lawesson's reagent, and 400 ml of toluene was refluxed for 1 hour. The reaction mixture was cooled to about 100° C. and then 300 ml of water was added. The resulting mixture was refluxed for 1 hour. The organic layer was separated, dried over magnesium sulfate, and concentrated to about 200 ml of volume. The precipitate was collected by filtration, washed with toluene, and dried to give 86.2 g of 4-trifluoromethyl-2'-methoxybenzothioanilide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06013659 |
|---|
| Source dataset | uspto-grants-2000_01 |
|---|
| ORD ID | ord-66f334df2f19436483adb0f166dec9ce |
|---|
| Source note | uspto-grants-2000_01 |
|---|