HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobutyrophenone → 2-(4-Chloro-1-phenyl-butylidene)-N-phenyl-hydrazinecarbothioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobutyrophenone | HCID 253533 | — |
| Reactant | Hydrazinecarbothioamide, N-phenyl- | HCID 730679 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Chloro-1-phenyl-butylidene)-N-phenyl-hydrazinecarbothioamide | HCID 53747260 | 62.6% |
Reaction Steps
A mixture of 4-chlorobutyrophenone (6.7 mL, 42 mmol) and 4-phenyl-3-thiosemicarbazide (7.0 g, 42 mmol) in 500 mL of ethanol was warmed under a nitrogen atmosphere to dissolve all the solids and then the reaction stirred at room temperature for four days. The solid formed was collected by filtration and dried under reduced pressure to give 8.73 g of a white solid. Recrystallization of the solid from ethanol gave 7.99 g (57%) of the title compound as a white solid, mp 107-109° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06008362 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-a4ace6d1b5ed443c8dd624f2fd2543b9 |
| Source note | uspto-grants-1999_12 |