HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253334Generated: November 2, 2026
HCID 21981744, compound → HCID 86741540, compound
https://huagongshe.com/reaction/1253334
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 21981744 | HCID 21981744 | — |
| Catalyst | 2-ethylhexanoic acid tin(II) salt | HCID 9318 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86741540 | HCID 86741540 | — |
Reaction Steps
In a one liter, 3-neck flask fitted with a mechanical stirrer, thermometer, condenser, gas inlet tube, addition funnel and electric heating mantle was placed 164g (0.34 mole) "Desmondur" N-100 biuret triisocyanate, and 109g ethyl acetate and 4 drops stannous octoate. The mixture was heated to 82° C. and stirred under a slow N2 stream while slowly adding over a period of 3 hours a solution of 319g (0.55 mole) N-ethyl (perfluorooctane) sulfonamidoethyl alcohol in 212g ethyl acetate and containing 3 drops of stannous octoate. Heating (82° C.) and stirring was continued for a period of 3 hours to yield mainly a fluorochemical biuret urethane isocyanate intermediate, (C8F17SO2N(C2H5)C2H4OCONHCO--2NC6H12NCO or more simply (Rf --Q--A--2B--A--NCO, and smaller amounts of B--A--Q--Rf)3 and (OCN--A--B--A--Q--Rf with B, A, Q and Rf as defined above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04748267 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-30a92c91f3164917b9dcd3f01056e4e9 |
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| Source note | uspto-grants-1988_05 |
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