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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212626Generated: November 2, 2026

Hydrogen Bromide → HCID 85829357, compound

https://huagongshe.com/reaction/2212626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantDiphenyl sulfideHCID 8766—
ReactantDiphenyl sulfoxideHCID 13679—
ReactantBromhydrolHCID 166749—
SolventAcetoneHCID 180—
SolventHexaneHCID 8058—
ProductHCID 85829357HCID 8582935778.3%

Reaction Conditions

Temperature5 °C

Reaction Steps

In 200 ml of n-hexane were suspended 6.07 g (0.03 mol) of diphenylsulfoxide and 11.2 g (0.06 mol) of diphenylsulfide, and 48.0 g (0.18 mol) of aluminum bromide was added thereto at 20 to 40° C., followed by reacting at 60 to 65° C. for 6 hours with stirring. After completion of the reaction, the reaction solution was poured into 500 ml of 12% hydrobromic acid, followed by washing with 200 ml of n-hexane five times and extracting with 200 ml of dichloromethane. The obtained dichloromethane layer was washed with 200 ml of water five times, followed by concentration under reduced pressure to obtain a crude product. Then, 120 ml of acetone was added to the crude product to dissolve at 55° C., followed by cooling to 5° C. to obtain crystal. The crystal was filtered off to obtain 5.3 g (Yield: 39%) of dipheny-4-phenylthiophenylsulfonium bromide as a pale yellow crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101918B2
Source datasetuspto-grants-2006_09
ORD IDord-c96cb19eefb54cdd967fcb4c0a1f4db7
Source noteuspto-grants-2006_09