HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452361Generated: October 23, 2026
Dimethylformamide → N,N,N',N',N''-Pentamethylguanidine
https://huagongshe.com/en/reaction/452361
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sulfuryl fluoride | HCID 17607 | — |
| Reactant | 1,1,3,3-Tetramethylguanidine | HCID 66460 | — |
| Product | N,N,N',N',N''-Pentamethylguanidine | HCID 139457 | — |
Reaction Steps
A perfluorinated polymer precursor (film thickness: 25 μm, sulfonyl fluoride form, EW1100) was treated with 1,1,3,3-tetramethylguanidine in dimethylformamide (DMF) solution at 90° C. for 24 hr. After washing with water, the membrane was dried under a vacuum plate at 75° C. The absorption by C═N was observed at 1525-1580 cm−1 by FT-IR, and C═N and N—CH3 peak was observed at 162 and 39.5 ppm by C-NMR, respectively. Tetramethlguanidine functionalized perfluorinated polymers were further treated with dimethyl sulfate (DMS) in DMF at 90° C. for 24 hr. Pentamethylguanidine functionalized perfluorinated polymer was obtained. Guanidine functionalized perfluorinated polymers were further treated with 1 M NaOH for 4 hr at boiling temperature followed by washing with water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08492049B2 |
|---|
| Source dataset | uspto-grants-2013_07 |
|---|
| ORD ID | ord-2d67d4c9922c4740991439bc2686c812 |
|---|
| Source note | uspto-grants-2013_07 |
|---|