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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372139Generated: October 27, 2026

Acetic Acid → Dimethyl 2-Oxo-3-methylheptylphosphonate

https://huagongshe.com/reaction/372139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantEthyl 2-methylhexanoateHCID 12714009—
ReactantButyllithiumHCID 178418339—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
ProductDimethyl 2-Oxo-3-methylheptylphosphonateHCID 1290667032.6%

Reaction Conditions

Temperature-60 °C

Reaction Steps

A stirred solution of dimethyl methylphosphonate (54 g.) in dry tetrahydrofuran (390 ml.) at -45° to -50° C. was treated, dropwise during 20 minutes, with a solution of butyl lithium (32 g.) in pentane (250 ml.). Stirring was continued at that temperature for a further 10 minutes, and then the mixture was cooled to -60° C. and treated, dropwise during 15 minutes, with a solution of ethyl 2-methylhexanoate (34.5 g.) in tetrahydrofuran (120 ml.). The mixture was stirred at -60° C. for a further 90 minutes and then at room temperature for 3 hours, and then it was treated with acetic acid (42 ml.), evaporated to dryness in vacuo, and the residue treated with water (170 ml.). The mixture was extracted twice with diethyl ether and the combined ethereal extracts washed with water, dried over sodium sulphate and evaporated to dryness in vacuo. The residue was distilled to give dimethyl 3-methyl-2-oxoheptylphosphonate (16.8 g.), b.p. 93-94° C./0.2 mm.Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04088821
Source datasetuspto-grants-1978_05
ORD IDord-6b5dc8e3ecda438f92757fcce2cbfcd0
Source noteuspto-grants-1978_05