HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041631Generated: October 26, 2026
Toluene → N,N,N',N'-tetramethylformamidinium para-toluenesulfonate
https://huagongshe.com/reaction/2041631
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 1-Pyrrolidinecarboxaldehyde | HCID 77372 | — |
| Product | N,N,N',N'-tetramethylformamidinium para-toluenesulfonate | HCID 86651391 | — |
Reaction Steps
A mixture of N-formylpyrrolidine (100 g) and dimethylsulfate (126 g) are heated to 80° C. for 4 h. Then a mixture of pyrrolidine (71 g) and toluene (100 ml) are added and the resulting mixture is stirred at reflux for 1 h. The reaction mixture is cooled to room temperature and the phases are separated. The lower layer is concentrated in vacuo and triturated with diethyl ester. The precipitate is collected by filtration and recrystallised using ethyl acetate to give 1-pyrrolidin-1-ylmethylene-pyrrolidinium methylsulfate (18, R6/R7=Pyrrolidinyl). 1H NMR (DMSO-d6), 8.28 (1H), 3.90-3.85 (4H), 3.68-3.62 (4H), 3.38 (3H), 1.99-1.90 (4H), 1.86-1.77 (4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580974B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-ccb2a3b269bd4b8b874f06316b192bb4 |
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| Source note | uspto-grants-2013_11 |
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