HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 23143326, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | N-[3-(Methylsulfanyl)propyl]thiourea | HCID 23143325 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 23143326 | HCID 23143326 | 70.1% |
Reaction Steps
A mixture of 2-bromo-1-phenylethanone (1.99 g), N-[3-(methylthio)propyl]thiourea (1.64 g) and N,N-dimethylformamide (5 mL) was stirred at room temperature for 1 hr. The reaction mixture was poured into water and extracted with ethyl acetate. The ethyl acetate layer was dried over anhydrous magnesium sulfate and concentrated to give the title compound (1.85 g, yield 70%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07585880B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-1de7ca53b86141d4883da887abcf1fe6 |
| Source note | uspto-grants-2009_09 |