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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867792Generated: October 29, 2026

Dimethyl methylphosphonate → HCID 14302187, compound

https://huagongshe.com/reaction/867792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl methylphosphonateHCID 12958—
ReactantBenzoic acid, 3-fluoro-, methyl esterHCID 521184—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14302187HCID 1430218783.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of dimethyl methylphosphonate (10.1 g, 81.2 mmol) in 100 ml of anhydrous THF was added dropwise n-butyl lithium (1.58N, 51.4 ml, 81.2 mmol) at -78° C. under argon atmosphere. After 30 minutes, methyl m-fluorobenzoate (5.0 g, 32 mmol) was further added dropwise and the mixture was stirred for 30 minutes. The reaction solution was allowed to warm to 0° C., diluted with 4.9 ml of acetic acid and 10 ml of water, and concentrated. 30 ml of water was added to the residue and the mixture was extracted with ethyl acetate (50 ml×2). The combined ethyl acetate layers were washed with water (20 ml×1) and brine (20 ml×1), dried over anhydrous sodium sulfate, and concentrated. The residue was distilled under reduced pressure to give an oil of dimethyl 2-m-fluorophenyl-2-oxo-ethylphosphonate (6.6 g, 26.8 mmol, yield 83.8%, b.p. 132°-134° C./0.17 mmHg), which was assigned the structure by the following data:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04775692
Source datasetuspto-grants-1988_10
ORD IDord-619b735a33c441c085d68bd7d074b4a7
Source noteuspto-grants-1988_10