HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901315Generated: October 25, 2026
1-Butanesulfonamide, 1,1,2,2,3,3,4,4,4-nonafluoro-N-(4-hydroxybutyl)-N-methyl- → C4F9SO2N(CH3)(CH2)11OH
https://huagongshe.com/reaction/901315
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanesulfonamide, 1,1,2,2,3,3,4,4,4-nonafluoro-N-(4-hydroxybutyl)-N-methyl- | HCID 69939 | — |
| Reactant | 11-Bromo-1-undecanol | HCID 74163 | — |
| Reactant | 1,1,2,2,3,3,4,4,4-nonafluoro-N-methylbutane-1-sulfonamide | HCID 109968 | — |
| Reactant | HCID 178418582 | HCID 178418582 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | C4F9SO2N(CH3)(CH2)11OH | HCID 131726834 | — |
Reaction Steps
C4F9SO2N(CH3)(CH2)11OH was prepared using a procedure similar to that described above for preparing C4F9SO2N(CH3)(CH2)4OH. 175.9 g C4F9SO2NHCH3 and 121.4 g 25% NaOCH3 were reacted to produce a solution of C4F9SO2NNaCH3 in about 100 mL diglyme. This solution was treated with 141 g 11-bromoundecanol (available from Aldrich) and heated at 100° C. for 20 hr to form a heavy precipitate. The reaction was quenched in about 600 mL warm water and the resulting lower layer was stripped at 50° C./0.5 mTorr to leave 269.9 g of C4F9SO2N(CH3)(CH2)11OH, a low-melting solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07361782B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-39c0e5cc0b934026948250077d6b552a |
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| Source note | uspto-grants-2008_04 |
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