HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057542Generated: October 31, 2026
Methyl iodide → Diethyl ({[(methylsulfanyl)carbonothioyl]amino}methyl)phosphonate
https://huagongshe.com/reaction/2057542
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Diethyl (aminomethyl)phosphonate | HCID 1596920 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Diethyl ({[(methylsulfanyl)carbonothioyl]amino}methyl)phosphonate | HCID 20330789 | — |
Reaction Steps
Carbon disulfide (0.88 ml, 1.11 g) was added dropwise to a stirred solution of 2.45 g (14.6 mmol) of diethyl aminomethylphosphonate and 0.82 g (14.6 mmol) of potassium hydroxide in 25 ml of ethanol. During addition the temperature of the reaction mixture rose from 26° to 33°. A second portion of 0.88 ml of carbon disulfide was added and the mixture was stirred at 50° for 1 hour. The mixture was cooled to ambient temperature, 2.08 g (14.6 mmol) of methyl iodide was added dropwise and the resulting mixture was stirred for 1.5 hours. The mixture was evaporated to dryness, the residue was dissolved in water and the aqueous solution was extracted twice with ethyl acetate. The extracts were combined, dried (MgSO4) and evaporated to dryness to give methyl 1-diethoxyphosphinylmethyldithiocarbamate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04211703 |
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| Source dataset | uspto-grants-1980_07 |
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| ORD ID | ord-76d02733418e4883a283cf2b56dd5446 |
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| Source note | uspto-grants-1980_07 |
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