HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284890Generated: October 31, 2026
Dimethyl Sulfoxide → HCID 86641513, compound
https://huagongshe.com/reaction/2284890
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-Chloroethyl vinyl ether | HCID 8074 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 18411305 | HCID 18411305 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86641513 | HCID 86641513 | 61.5% |
Reaction Steps
A 3-neck-round bottom flask was fitted with a condenser, an addition funnel, nitrogen source, and a magnetic bar. Sodium hydroxide (8.64 g, 0.216 mol), bis(4-hydroxyphenyl)phenylsulfonium triflate (16 g, 0.036 mol) and DMSO (90 ml) were added to a round bottom flask under N2. The mixture was heated to 60° C. for 1 hour. 2-chloroethyl vinylether (23 g, 0.216 mol) was added dropwise to the mixture via the addition funnel. The temperature was then increased to 80° C. and the reaction was held at that temperature for 5 hours. The reaction mixture was then allowed to cool down to room temperature. Thereafter, the reaction mixture was poured into diethyl ether to form three layers: aqueous, ether, and an oil. DI water was used to wash the ether solution 3 times. An oily layer was collected and concentrated to dryness. 12.9 g (61.5%) of bis(4-vinyloxyethyloxyphenyl)phenylsulfonium triflate was obtained. The structure was confirmed using 1H and 19F NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09146467B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-8976ffb818c24ffabc4a1f4b02079731 |
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| Source note | uspto-grants-2015_09 |
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