HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486439Generated: October 29, 2026
2,6-Lutidine → 3-Fluoropropyl trifluoromethanesulfonate
https://huagongshe.com/reaction/1486439
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 3-Fluoro-1-propanol | HCID 68042 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Fluoropropyl trifluoromethanesulfonate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09427442B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-56872bc9033044b39f79db77d0a725d9 |
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| Source note | uspto-grants-2016_08 |
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