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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexane | HCID 8058 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Methyl 3-chlorobenzoate | HCID 17946 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Dimethyl 2-m-chlorophenyl-2-oxoethylphosphonate | HCID 14302190 | 84.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04775692 |
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| Source dataset | uspto-grants-1988_10 |
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| ORD ID | ord-759f6c2f77a048ea9a7c870fd62d0f7d |
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| Source note | uspto-grants-1988_10 |
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