HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388279Generated: November 3, 2026
1,3-Propanediamine → HCID 20470672, compound
https://huagongshe.com/reaction/1388279
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Propanediamine | HCID 428 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | 1-Hexanesulfonyl fluoride, 1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluoro- | HCID 67918 | — |
| Product | HCID 20470672 | HCID 20470672 | 99.6% |
Reaction Steps
111 g (1.5 moles) of 1,3-diaminopropane and 300 g of fully dehydrated isopropyl ether were weighed in an atmosphere of nitrogen into a 2-liter three-necked round-bottomed flask equipped with a cooling condenser and stirrer. With sufficient stirring, 237 g (0.59 mole) of perfluorohexyl sulfonyl fluoride was added dropwise at room temperature from a dropping funnel. The mixture was stirred at 50° C. for 3 hours, and then the isopropyl ether was removed under reduced pressure. The oily residue was dissolved in 200 ml of ethanol, and gradually poured into 5 liters of distilled water with stirring. The resulting crystals were aged. The supernatant liquid was removed by decantation, and 1 liter of 0.5 N aqueous sodium hydroxide solution was added to wash the crystals. Decantation was performed for three more times using 5 liters of distilled water each time. The crystals were collected by filtration, washed with distilled water and dried at 60° C. under reduced pressure. There was obtained 268 g of N-(3 -aminopropyl)perfluorohexyl sulfonamide having a sufficient purity for use in the subsequent reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04431595 |
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| Source dataset | uspto-grants-1984_02 |
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| ORD ID | ord-88bd85b9fd5c4b5e905369d3e3cf8549 |
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| Source note | uspto-grants-1984_02 |
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