HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944993Generated: October 26, 2026
Dimethylamine → ethyl 4-(N,N-dimethylamidino)benzoate
https://huagongshe.com/reaction/1944993
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Ethyl 4-cyanobenzoate | HCID 81589 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178506865 | HCID 178506865 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | ethyl 4-(N,N-dimethylamidino)benzoate | HCID 22631319 | — |
Reaction Steps
To a tetrahydrofuran solution of 2M dimethylamine, 2.3M hexane solution of hexyllithium was slowly added over a period of at least three (3) hours while maintaining the temperature at between −8° C. and −12° C. This solution was added to the tetrahydrofuran solution of ethyl-4-cyanobenzoate (F) while maintaining the temperature between −8° C. and −12° C. The completion of the reaction was confirmed by HPLC, and the solution temperature was adjusted to between −8° C. and 3° C. The reaction mixture was slowly added to the cold solution of aqueous sodium bicarbonate solution and the desired ethyl-4-(N,N-dimethylcarbamimidoyl)benzoate (G) was extracted with ethyl acetate. The ethyl acetate layer was dried, filtered and evaporated under vacuum to afford ethyl-4-(N,N-dimethylcarbamimidoyl)benzoate (G) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394964B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-92f64938518e401eb008190759f2ff0d |
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| Source note | uspto-grants-2013_03 |
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