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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414584Generated: October 31, 2026

Trimethyl phosphite → HCID 21281101, compound

https://huagongshe.com/reaction/414584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl phosphiteHCID 8472—
ReactantEthyl chloroformateHCID 10928—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 54414975HCID 54414975—
SolventChloroformHCID 6212—
ProductHCID 21281101HCID 21281101—

Reaction Conditions

Temperature-5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04792567
Source datasetuspto-grants-1988_12
ORD IDord-6089359337df406985f82a93eee5e1ec
Source noteuspto-grants-1988_12