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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351053Generated: November 2, 2026

Water → 4-n-Butanesulfonyloxyphenyl diphenylsulfonium nonafluoro-n-butanesulfonate

https://huagongshe.com/reaction/1351053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant1-Butanesulfonyl chlorideHCID 75430—
ReactantHCID 22481373HCID 22481373—
SolventDichloromethaneHCID 6344—
Product4-n-Butanesulfonyloxyphenyl diphenylsulfonium nonafluoro-n-butanesulfonateHCID 8659678873.7%

Reaction Steps

30 g of 4-hydroxyphenyl diphenylsulfonium nonafluoro-n-butanesulfonate was dissolved in 300 g of dichloromethane in a reaction flask, in which the atmosphere was replaced with nitrogen. 17.9 g of n-butanesulfonyl chloride and 10.5 g of triethylamine were added in this order. The mixture was stirred for 20 minutes at room temperature. After the addition of 100 g of ion-exchanged water, the mixture was transferred to a separatory funnel, shaken, and allowed to stand still. The water layer was removed. After the addition of 300 ml of distilled water, the solution was shaken and allowed to stand still. The water layer was removed. The resulting dichloromethane solution was dried using anhydrous magnesium sulfate and filtered. After evaporating dichloromethane from the dichloromethane solution, the residual liquid was dried under reduced pressure to obtain 26.7 g of 4-n-butanesulfonyloxyphenyl diphenylsulfonium nonafluoro-n-butanesulfonate. This compound is indicated as “acid generator (A-1)”.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217492B2
Source datasetuspto-grants-2007_05
ORD IDord-bf06902f67be405c9d048e256c4a904b
Source noteuspto-grants-2007_05