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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Ethyl 2-cyclohexylpropionate | HCID 160641 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Dimethyl 3-cyclohexyl-2-oxobutylphosphonate | HCID 21516126 | 30.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03978229 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-8caf455991bd442999f97627902fd15a |
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| Source note | uspto-grants-1976_08 |
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