HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thioacetamide → 2-Methyl-5,6-dihydrobenzo[d]thiazol-7(4H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thioacetamide | HCID 2723949 | — |
| Reactant | 2-Bromocyclohexane-1,3-dione | HCID 2770476 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Methyl-5,6-dihydrobenzo[d]thiazol-7(4H)-one | HCID 14913369 | — |
Reaction Steps
To a solution of ethanethioamide (0.75 g, 10 mmol) in ethanol (20 mL) at room temperature was added 2-bromocyclohexane-1,3-dione (1.9 g, 10 mmol) in portions. The reaction solution was refluxed for 2 hours while stirring. After removal of solvents, the residue was diluted with water and washed with diethyl ether. The separated aqueous layer was basified with sodium carbonate solution. The resulting solid was collected by vacuum filtration, rinsed with water. The solid was suspended in methanol and followed by evaporation to dryness to produce the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08710245B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-ce6dc72c650a4d18bcf495da9bdd852e |
| Source note | uspto-grants-2014_04 |