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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284314Generated: October 27, 2026

Dimethyl methylphosphonate → Dimethyl 3-cyclohexyl-2-oxobutylphosphonate

https://huagongshe.com/reaction/1284314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl methylphosphonateHCID 12958—
ReactantEthyl 2-cyclohexylpropionateHCID 160641—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductDimethyl 3-cyclohexyl-2-oxobutylphosphonateHCID 2151612630.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

74.5 g. of dimethyl methylphosphonate were dissolved in 514 ml. of tetrahydrofuran and the solution cooled to -60°C. To this solution a solution of n-butyl-lithium [prepared from 40.5 g. of n-butyl bromide and 9.2 g. of lithium] in 240 ml. of diethyl ether was added dropwise. A solution of 39.5 g. of ethyl 2-cyclohexylpropionate in 130 ml. of tetrahydrofuran was added dropwise and the mixture stirred at the same temperature for 2 hours and afterwards at 0°C. overnight. The reaction mixture was then neutralized to pH 7 with acetic acid, concentrated under reduced pressure and, after the addition of water to the residue, extracted with diethyl ether. After drying the ethereal extract, the solvent was distilled off and the residue subjected to distillation under reduced pressure to obtain 40 g. (yield 30.2 %) of the title compound as a colourless oil having the following physical characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03978229
Source datasetuspto-grants-1976_08
ORD IDord-8caf455991bd442999f97627902fd15a
Source noteuspto-grants-1976_08