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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867797Generated: October 26, 2026

Hexane → Dimethyl 2-m-chlorophenyl-2-oxoethylphosphonate

https://huagongshe.com/reaction/867797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantMethyl 3-chlorobenzoateHCID 17946—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductDimethyl 2-m-chlorophenyl-2-oxoethylphosphonateHCID 1430219084.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of n-butyl lithium in hexane (1.63N, 45 ml, 73.3 mmol) was added dropwise to a solution of dimethyl methylphosphonate (9.1 g, 73.3 mmol) in 100 ml of anhydrous THF with stirring at -78° C. under argon atmosphere, and the mixture was stirred for 30 minutes. Then, methyl m-chlorobenzoate (5.0 g, 29.3 mmol) in 10 ml of anhydrous THF was further added dropwise and the mixture was stirred for 30 minutes. This reaction mixture was allowed to warm to 0° C., diluted with 4.4 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 (30 ml×1) and brine (30 ml×1), dried over anhydrous sodium sulfate, and concentrated. The residue was distilled under reduced pressure to give a colorless transparent oil of dimethyl 2-m-chlorophenyl-2-oxoethylphosphonate (6.5 g, 24.8 mmol, yield 84%, b.p. 144°-146° C./0.06 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-759f6c2f77a048ea9a7c870fd62d0f7d
Source noteuspto-grants-1988_10