HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-4'-methylbutyrophenone → 2-[1-(4-Methyl-phenyl)-4-chloro-butylidene]-hydrazinecarbothioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-4'-methylbutyrophenone | HCID 98745 | — |
| Reactant | Thiosemicarbazide | HCID 2723789 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[1-(4-Methyl-phenyl)-4-chloro-butylidene]-hydrazinecarbothioamide | HCID 54127402 | 75.2% |
Reaction Steps
Thiosemicarbazide (6.84 g, 75 mmol) was added under nitrogen to a solution of 4-chloro-4'-methylbutyrophenone (10.0 g, 50 mmol) in 175 mL of methanol plus 13.5 mL of 1 N HCl plus 12.5 mL of water and the reaction stirred at room temperature overnight. The solid formed was collected by filtration and dissolved in methylene chloride. The organic solution was washed multiple times with water, dried (MgSO4) and the solvent removed under reduced pressure to give 10.15 g of an off-white solid. Recrystallization of the solid from isopropyl alcohol gave 8.65 g (64%) of the tide compound as an off-white solid, mp133-135° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06008362 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-5f1abbbe2bbd47828c907cf2310e5e60 |
| Source note | uspto-grants-1999_12 |