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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596781Generated: November 1, 2026

4-Toluenesulfonyl chloride → 5-Fluoro-3-(3-p-toluenesulfonyloxypropyl)indole

https://huagongshe.com/reaction/1596781

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant3-(5-fluoro-1H-indol-3-yl)propan-1-olHCID 15020541—
SolventPyridineHCID 1049—
Product5-Fluoro-3-(3-p-toluenesulfonyloxypropyl)indoleHCID 1502054279%

Reaction Steps

To a stirred solution of 3-(5-fluoro-1H-indol-3-yl)-propan-l-ol (2.90 g, 15.0 mmol) in pyridine (15.0 mL) was added p-toluenesulfonyl chloride (7.1 g, 37.5 mmol) at room temperature. After stirring for 30 minutes at room temperature, the reaction mixture was poured to 200 nm of ice water. The aqueous was extracted with ethyl acetate and the combined organic extracts were washed with IN HCI and brine. The resulting material was dried over anhydrous sodium sulfate, filtered, and the solvent was concentrated under vacuum. The crude product was purified by silica gel column chromatography (ethyl acetatehexane, 3n) to give 4.1 g (79%) of the title compound as a solid: mp 74 CC (Lit. mp 99 ° C.; EP 464604 A2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291683B1
Source datasetuspto-grants-2001_09
ORD IDord-ac37f212a5d84d8ebf7481c256366770
Source noteuspto-grants-2001_09