HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31665Generated: October 25, 2026
1,1,2,2,3,3,4,4,4-Nonafluorobutane-1-sulfonyl chloride → (2-(Fluoromethyl)-1,3-dioxan-2-yl)methyl benzoate
https://huagongshe.com/reaction/31665
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1,2,2,3,3,4,4,4-Nonafluorobutane-1-sulfonyl chloride | HCID 324955 | — |
| Reactant | HCID 59792406 | HCID 59792406 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (2-(Fluoromethyl)-1,3-dioxan-2-yl)methyl benzoate | HCID 59792542 | 46.4% |
Reaction Steps
To a toluene (100 ml) solution of (2-(hydroxymethyl)-1,3-dioxan-2-yl)methyl benzoate (4.76 g, 18.8 mmol), 1,8-diazabicyclo[5.4.0]unedec-7-ene (8.43 ml, 56.4 mmol) was added, cooled on ice and nonafluoro-1-butanesulfonyl chloride (5.06 ml, 28.2 mmol) was added. The mixture was stirred under ice-cool for 15 minutes, and at 40° C. for 20 hours, and further stirred at room temperature for 8 days. The reaction mixture was extracted by adding water and ethyl acetate. The organic layer was washed with a saturated saline solution, dried over magnesium sulfate, and filtrated through silica gel, and then, the filtrate was concentrated. The residue was subjected twice to silica gel column chromatography (elution solvent: n-heptane/ethyl acetate=4/1) to obtain the title compound (2.22 g, yield: 46.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07425634B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-a46f58d7a1c84f10999d20f55d0309d4 |
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| Source note | uspto-grants-2008_09 |
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