HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiourea → p-Toluenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | HCID 11666101 | HCID 11666101 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | p-Toluenesulfonate | HCID 85570 | 174.8% |
| Product | 4,4-Difluorobut-3-enylthiourea | HCID 21478900 | — |
Reaction Steps
Thiourea (0.29 g) and 4,4-difluorobut-3-enyl 4-methyl-benzenesulfonate (1 g) were heated together under reflux in ethanol (20 cm3) for 24 hours. The reaction mixture was cooled and the solvent evaporated under reduced pressure to give an oil which slowly crystallised. Trituration with hexane gave (4,4-difluorobut-3-enyl)-thiourea as its 4-methyl-benzenesulfonate salt (1.14 g). MH+ (FAB)=167; 1H NMR (DMSO-d6): δ 2.48(3H,s); 2.46-2.58(2H,m); 3.42(2H,t); 4.66-4.84(1H,m); 7.32(2H,d); 7.68(2H,d); 9.10-9.40(3H,br).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05952359 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-52a89cd40f7e4133bc288de8841ceed8 |
| Source note | uspto-grants-1999_09 |