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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397649Generated: October 25, 2026

Sodium Carbonate → C4F9SO2-N(CH3)CH2CH2-NH2

https://huagongshe.com/reaction/1397649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Ethyl-2-oxazolineHCID 66412—
Reactant1,1,2,2,3,3,4,4,4-nonafluoro-N-methylbutane-1-sulfonamideHCID 109968—
ProductC4F9SO2-N(CH3)CH2CH2-NH2HCID 86649493—
ProductN-(2-(N-methylnonafluorobutanesulfonamido)ethyl)propionamideHCID 86657621—

Reaction Conditions

Temperature140 °C

Reaction Steps

C4F9SO2—N(CH3)CH2CH2—NH2 was prepared by the following procedure: N-Methylnonafluorobutanesulfonamide (626 g, 2 moles, 3M Company, St. Paul, Minn.), 2-ethyl-2-oxazoline (198 g, 2 moles, Alfa Aesar, Ward Hill, Mass.), and sodium carbonate (17 g, 0.16 mole, EMD Chemicals, Gibbstown, N.J.) were combined and heated for 16 hours at 140° C. to form N-(2-(N-methylnonafluorobutanesulfonamido)ethyl)propionamide. This amide was twice extracted with 250 mL deionized water, heated for 18 hours at 100° C. with a mixture of 250 mL concentrated hydrochloric acid and 100 mL deionized water, extracted with 925 mL of 24 weight percent aqueous sodium hydroxide solution, extracted with 250 mL 10 weight percent aqueous sodium hydroxide solution, and distilled to provide N-(2-aminoethyl)-N-methylnonafluorobutanesulfonamide (538 g; 75 percent recovery; 94 percent pure by gas chromatography (GC); distilled at 104-109° C. under 2 mm Hg pressure).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901263B2
Source datasetuspto-grants-2014_12
ORD IDord-a490c14836694b45b24b0ad807c3579c
Source noteuspto-grants-2014_12