HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-1-(2-thienyl)butan-1-one → 2-[4-Chloro-1-(thiophen-2-yl)-butylidene]-hydrazinecarbothioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-1-(2-thienyl)butan-1-one | HCID 123511 | — |
| Reactant | Thiosemicarbazide | HCID 2723789 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[4-Chloro-1-(thiophen-2-yl)-butylidene]-hydrazinecarbothioamide | HCID 54569609 | 57% |
Reaction Steps
Thiosemicarbazide (9.11 g, 0.1 mol) was added under nitrogen to a solution 4-chloro-2'-butyrothienone (16.2 mL, 0.1 mol) in 350 mL of methanol plus 27 mL 1N HCl plus 25 mL of water. After stirring at room temperature for approximately 2 hours, all of the solid had dissolved. The reaction was then stirred at room temperature for 24 hours (overnight). By TLC starting material remained. An additional 27 mL of 1N HCl was added and the reaction stirred at room temperature for 6 hours. The solid formed was removed by filtration and dried under high vacuum to give 14.87 g (57%) of the title compound as a brown solid, mp 120-122° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06008362 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-08f667f3cc214dae90b9d0e45627e7c1 |
| Source note | uspto-grants-1999_12 |