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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599191Generated: October 27, 2026

4-Toluenesulfonyl chloride → 2-Fluoroethyl p-Toluenesulfonate

https://huagongshe.com/reaction/599191

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant2-FluoroethanolHCID 9737—
SolventPyridineHCID 1049—
Product2-Fluoroethyl p-ToluenesulfonateHCID 25601995%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. solution of 2-fluoroethanol (1.0 g, 15.6 mmol) in pyridine (15 mL) was added tosyl chloride (6.5 g, 34.1 mmol) over 30 min. The reaction mixture was stirred at 0° C. for 4 h and quenched by adding ice-cold water and EtOAc. The layers separated and the organic layer was washed successively with water, 1M HCl (5×), saturated Na2CO3 and brine. The organic layer was dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The residue was chromatographed on silica gel (12 g) using 5% to 40% EtOAc in hexane as the eluant to obtain fluorotosylate 20 (3.2 g, 95%) as a slightly yellow oil. 1H NMR (500 MHz, CDCl3) δ 7.83 (d, J=10.0 Hz, 1H), 7.38 (d, J=10.0 Hz, 2H), 4.59 (dt, J=50.0 & 5.0 Hz, 2H), 4.28 (dt, J=30.0 & 5.0 Hz, 2H), 2.47 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897769B2
Source datasetuspto-grants-2011_03
ORD IDord-560ca48835c6429fb0777279549ea3de
Source noteuspto-grants-2011_03