HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584683Generated: November 4, 2026
Isopropylammonium chloride → HCID 21219670, compound
https://huagongshe.com/reaction/1584683
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropylammonium chloride | HCID 27399 | — |
| Reactant | Diethyl cyanophosphonate | HCID 76257 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21219670 | HCID 21219670 | 88% |
Reaction Steps
Diethyl cyanophosphonate (0.50 g, 3.06 mmol) and isopropylammonium chloride (0.29 g, 3.03 mmol) were added to DMF (3 mL) and the reaction mixture was stirred overnight. The solvent was removed under reduced pressure to give 0.48 g (88% yield) of an oil which was analyzed by NMR and mass spectrometry without additional purification. 31P NMR (CD2Cl2) δ (ppm) -21.2 (t, 3JPH =8.4 Hz); 13C NMR (CD2Cl2) δ (ppm) 121.0 (d, 1JCP =177.8 Hz), 63.2 (d, 2JCP 6.3 Hz), 42.1 (s), 20.9 (s), 16.0 (d, 3JCP =7.5 Hz). Mass spectral analysis (FAB+TGL) detected the peak at m/z 195, corresponding to the protonated form of the salt [+NH3CH(CH3)2 --O(OC2H5)POCN+H+ ], the presence of the cation at m/z 60 ([NH3CH(CH3)2 ]+) and an anionic species (FAB-, TGL) at m/z 134 [NCP(O)(OC2H5)O- ].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05935542 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-30370708927e420fa16e0c7c8f1c7657 |
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| Source note | uspto-grants-1999_08 |
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