HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395394Generated: October 31, 2026
Carbon Tetrachloride → 1-Acetyl-1-Methyl-2-Diethoxyphosphoryl Hydrazine
https://huagongshe.com/reaction/1395394
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Acetic acid, 1-methylhydrazide | HCID 19051 | — |
| Reactant | Diethylphosphite | HCID 3780918 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Acetyl-1-Methyl-2-Diethoxyphosphoryl Hydrazine | HCID 20339292 | — |
Reaction Steps
A mixture of 1-acetyl-1-methyl hydrazine (7.84 g., 0.09 mole), potassium carbonate (18.44 g., 0.13 mole) and triethylbenzyl ammonium chloride (0.2 g,) was stirred vigorously at reflux with dichloromethane (90 ml) and carbon tetrachloride (55 ml) for 30 minutes. A solution of diethylphosphite (12.29 g, 0.09 mole) in dichloromethane (18 ml) was then added dropwise to this refluxing mixture and the mixture stirred and refluxed for an additional 20 hours. The mixture was then filtered and the filtrate dried over anhydrous magnesium sulfate. The dried filtrate, then was evaporated down to an oil which was subjected to high vacuum for 2 or 3 hours to yield a liquid product, characterized by proton NMR, infra-red and mass spectroscopy as the subject compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04203932 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-a6ef4567212946678b0b7496963aeee6 |
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| Source note | uspto-grants-1980_05 |
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