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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253389Generated: November 1, 2026

Dimethyl Sulfoxide → HCID 86641513, compound

https://huagongshe.com/reaction/1253389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDiethyl EtherHCID 3283—
Reactant2-Chloroethyl vinyl etherHCID 8074—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 18411305HCID 18411305—
SolventWaterHCID 962—
ProductHCID 86641513HCID 8664151361.5%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455176B2
Source datasetuspto-grants-2013_06
ORD IDord-529e9e2e634f43d48d6a215ea83c2ee9
Source noteuspto-grants-2013_06