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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351055Generated: November 3, 2026

Butanethiol → HCID 87870791, compound

https://huagongshe.com/reaction/1351055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanethiolHCID 8012—
ReactantSodium HydroxideHCID 14798—
Reactant(4-Fluorophenyl)(diphenyl)sulfanium trifluoromethanesulfonateHCID 16213837—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDichloromethaneHCID 6344—
ProductHCID 87870791HCID 8787079157.3%

Reaction Steps

26.7 g of 4-fluorophenyl diphenylsulfonium trifluoromethanesulfonate was dissolved in 200 g of dichloromethane in a reaction flask, in which the atmosphere was replaced with nitrogen. 200 g of 10 wt % sodium hydroxide aqueous solution, 5.8 g of tetra-n-butylammonium bromide, and 6.71 g of n-butanethiol were added. The mixture was stirred for 30 minutes at room temperature and 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 mixture was shaken and allowed to stand still. The water layer was removed. The resulting dichloromethane solution was dried with anhydrous magnesium sulfate, filtered, and dried using an evaporator. After evaporating dichloromethane from the dried solution, the residual liquid was dried under reduced pressure to obtain 17.8 g of 4-n-butylthiophenyl diphenylsulfonium trifluoromethanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217492B2
Source datasetuspto-grants-2007_05
ORD IDord-6991987230394638a63283bdebfc4826
Source noteuspto-grants-2007_05