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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Butanesulfonamide, 1,1,2,2,3,3,4,4,4-nonafluoro-N-(4-hydroxybutyl)-N-methyl-HCID 69939—
Reactant11-Bromo-1-undecanolHCID 74163—
Reactant1,1,2,2,3,3,4,4,4-nonafluoro-N-methylbutane-1-sulfonamideHCID 109968—
ReactantHCID 178418582HCID 178418582—
SolventDiglymeHCID 8150—
ProductC4F9SO2N(CH3)(CH2)11OHHCID 131726834—

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361782B2
Source datasetuspto-grants-2008_04
ORD IDord-39c0e5cc0b934026948250077d6b552a
Source noteuspto-grants-2008_04