HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335350Generated: October 30, 2026
Carbon Disulfide → HCID 17866105, compound
https://huagongshe.com/reaction/335350
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | p-Vinylbenzyl chloride | HCID 74126 | — |
| Product | HCID 17866105 | HCID 17866105 | — |
| Product | HCID 86654443 | HCID 86654443 | — |
Reaction Steps
4-vinylbenzyl dithiobenzoate (VBThB) was prepared according to reaction scheme 4, as follows. A 500 mL round bottom flask was dried with 3 vacuum/heat/nitrogen cycles. 100 mL of dry THF was added along with 3.3 grams of magnesium turnings. The mixture was placed in an oil bath set to 40° C., and 13.8 grams (0.088 moles) bromobenzene was added. 7.91 mL (0.088 moles) of dry carbon disulfide was added dropwise over the next 15 minutes. When all the carbon disulfide was added, the temperature was increased to 50° C., and 18.62 grams (0.088 moles) of 4-vinylbenzyl chloride was added. The solvent was removed. The crude product was purified via column chromatography over activated alumina (Brockman activity II). The final product was obtained as a red oil. The conversion was estimated at 48% after eluent removal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883912B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-63aa2bfd23c04708b1f47e88d539f1a5 |
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| Source note | uspto-grants-2014_11 |
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