HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Disulfide → HCID 86612043, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Bromobenzyl Cyanide | HCID 22044 | — |
| Reactant | HCID 178418423 | HCID 178418423 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86612043 | HCID 86612043 | — |
Reaction Steps
To a 100 ml round bottom flask was added 20 ml 2-naphthylmagnesium bromide (0.5M solution in THF). 0.76 g carbon disulfide was added dropwise to this mixture and stirred for ½ h at room temperature. Then to the dark red solution was added 2 g α-bromobenzeneacetonitrile dropwise and the mixture stirred for another 2 h. Water was added to the mixture and the organic product was extracted with diethyl ether (3×50 ml), dried with magnesium sulfate overnight and filtered. After removal of solvent and column chromatography (10:3 mixture of hexane and ethyl ether), pure α-cyanobenzyl dithionaphthalate was obtained as an orange odorless solid (63% yield). Proton and carbon NMR spectra were consistent with the expected structure, CTA-CP-2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07332552B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-6df41bc16a104440a1a018e2575d842b |
| Source note | uspto-grants-2008_02 |