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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046552Generated: October 25, 2026

p-Toluenesulfonic acid monohydrate → 2-(5-Bromoindane-1-ylidene)-1,3-dithiane

https://huagongshe.com/reaction/2046552

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant5-bromo-1-(1,3-dithian-2-yl)-2,3-dihydro-1H-inden-1-olHCID 57419484—
SolventBenzeneHCID 241—
Product2-(5-Bromoindane-1-ylidene)-1,3-dithianeHCID 57419485—

Reaction Steps

A mixture of (rac)-5-bromo-1-[1,3]dithian-2-yl-indan-1-ol (2.15 g, 6.49 mmol) and p-toluenesulfonic acid monohydrate (309 mg, 1.62 mmol) in benzene (30 ml) was heated to reflux for 2 h using a Dean-Stark trap to remove water. The brown solution was allowed to cool to room temperature and was diluted with sat. NaHCO3 solution. The layers were separated and the organic layer was washed with brine, dried with Na2SO4 and evaporated. The title compound was obtained as brown gum (2.024 g, 99%) and was used without purification for the next reaction step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592426B2
Source datasetuspto-grants-2013_11
ORD IDord-074c5ef97fa1482094f2dbc5e672e221
Source noteuspto-grants-2013_11