HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414584Generated: October 31, 2026
Trimethyl phosphite → HCID 21281101, compound
https://huagongshe.com/reaction/414584
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyl phosphite | HCID 8472 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 54414975 | HCID 54414975 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21281101 | HCID 21281101 | — |
Reaction Steps
The solution of N-(cyclohexylmethyl)phenylmethanimine in chloroform was diluted to 100 mL with fresh chloroform. This solution was stirred and cooled to -5° C. Ethyl chloroformate (11.0 mL, 0.12 mole) was added, and the mixture was stirred for ten minutes. Trimethyl phosphite (13.0 mL, 0.11 mole) was added, and the cold mixture was stirred for an additional ten minutes. The mixture was allowed to warm to room temperature and stir for 30 minutes. This mixture was poured slowly into an aqueous solution of potassium carbonate. The resultant mixture was extracted with chloroform. The extract was washed with an aqueous solution saturated with sodium chloride and then was dried over anhydrous magnesium sulfate. The dried solution was filtered, and the filtrate was evaporated under reduced pressure, leaving an oil. This oil was purified by column chromatography on silica gel to yield ethyl N-cyclohexylmethyl-N-[phenyl(dimethoxyphosphinyl)methyl]carbamate as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04792567 |
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| Source dataset | uspto-grants-1988_12 |
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| ORD ID | ord-6089359337df406985f82a93eee5e1ec |
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| Source note | uspto-grants-1988_12 |
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