HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium sulfide nonahydrate → 4-(4,4-Difluoro-but-3-enyldisulfanyl)-1,1-difluoro-but-1-ene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium sulfide nonahydrate | HCID 73972 | — |
| Reactant | Sodium disulfide | HCID 89870 | — |
| Reactant | 4-Bromo-1,1-difluorobut-1-ene | HCID 2782240 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(4,4-Difluoro-but-3-enyldisulfanyl)-1,1-difluoro-but-1-ene | HCID 21712911 | — |
Reaction Steps
A solution of sodium disulfide (previously prepared from sodium sulfide nonahydrate (53 g) and sulfur (7.0 g) in ethanol (250 cm3)) was added to 1-bromo4,4-difluorobut-3-ene (50 g) in ethanol (100 cm3). The mixture was gradually heated and stirred under reflux for 2 hours, then cooled and evaporated under reduced pressure. The residue was extracted with diethyl ether, the organic phase filtered to remove sodium bromide and the ether evaporated under reduced pressure to give a liquid which was distilled at 16 mm Hg, bp 120° C. to give the bis-(4,4-difluorobut-3-enyl)disulfide (24 g) as a colourless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06274632B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-3475dfc603334e56b64100cc5912dc74 |
| Source note | uspto-grants-2001_08 |