HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886130Generated: November 1, 2026
Sodium hexafluoroantimonate → Dibenzyl(phenyl)sulfanium hexafluoroantimonate(1-)
https://huagongshe.com/reaction/1886130
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hexafluoroantimonate | HCID 16689647 | — |
| Reactant | HCID 19877065 | HCID 19877065 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Dibenzyl(phenyl)sulfanium hexafluoroantimonate(1-) | HCID 21263248 | 191.3% |
Reaction Steps
A mixture of 123.0 g (0.325 mol) of dibenzylsulfonium tetrafluoroborate in 400 ml of methylene chloride is dissolved in a 2 liter round-bottomed flask at RT under N2 to give a clear solution. 117.8 g of sodium hexafluoroantimonate are then added and the mixture is stirred at RT for 31/2 h. The suspension is now filtered over silica gel and the solvent is removed from the filtrate using a rotary evaporator. The slightly reddish viscous residue is dissolved again in 250 ml of methanol, and after addition of 250 ml of water the product is allowed to crystallize at RT for 1-2 h. The suspension is filtered and the residue is washed with water. The product is then dried under a high vacuum at RT overnight. 163.9 g (95% of theory) of dibenzylphenylsulfonium hexafluoroantimonate are obtained as white crystals of melting point 105°-109° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05149767 |
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| Source dataset | uspto-grants-1992_09 |
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| ORD ID | ord-758fbc23794545e98acc52c60347c6e6 |
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| Source note | uspto-grants-1992_09 |
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