Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486439Generated: October 29, 2026

2,6-Lutidine → 3-Fluoropropyl trifluoromethanesulfonate

https://huagongshe.com/reaction/1486439

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant3-Fluoro-1-propanolHCID 68042—
SolventDichloromethaneHCID 6344—
Product3-Fluoropropyl trifluoromethanesulfonateHCID 44717394—

Reaction Steps

To a cold (−25° C.), stirred solution of 2,6-lutidine (4.60 mL, 39.5 mmol) in DCM (30 mL) was added triflic anhydride (6.00 mL, 35.5 mmol) over 3 min. Then 3-fluorpropane-1-ol (Oakwood, cat. 010306-25G, 1.61 g, 20.6 mmol) was added. The reaction mixture was warmed to room temperature for 2.5 h. The reaction mixture was concentrated to half its volume and purified by flash chromatography (Teledyne ISCO CombiFlash, isocratic DCM, REDISEP® SiO2 120 g, detecting at 254 nM, and monitoring at 220 nM). Concentration of the appropriate fractions provided Intermediate S-6A (2.92 g, 67.4%). 1H NMR (400 MHz, chloroform-d) δ ppm 4.69 (2H, t, J=6.16 Hz), 4.65 (1H, t, J=5.50 Hz), 4.54 (1H, t, J=5.61 Hz), 2.25 (1H, dt, J=11.39, 5.86 Hz), 2.19 (1H, dt, J=11.44, 5.94 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09427442B2
Source datasetuspto-grants-2016_08
ORD IDord-56872bc9033044b39f79db77d0a725d9
Source noteuspto-grants-2016_08