HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389029Generated: November 1, 2026
Acetic Acid → Dimethyl 2-oxo-2-phenylethylphosphonate
https://huagongshe.com/reaction/1389029
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | CID 406 | HCID 406 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Dimethyl 2-oxo-2-phenylethylphosphonate | HCID 569473 | 29% |
Reaction Steps
A solution of 74.5 g (600 mmoles) dimethyl methylphosphonate (Aldrich) in 750 ml dry tetrahydrofuran was cooled to -78° in a dry nitrogen atmosphere. To the stirred phosphonate solution was added 265 ml of 2.34 M n-butyllithium in hexane solution (Alfa Inorganics, Inc.) dropwise over a period of 30 minutes at such a rate that the reaction temperature never rose above -65°. After an additional 5 minutes stirring at -78°, 41 g (300 mmole) of methyl azoate was added dropwise at a rate that kept the reaction temperature less than -70° (10 minutes). After 1 hour at -78° the reaction mixture was allowed to warm to ambient temperature, neutralized with 35 ml acetic acid and rotary evaporated to a white gel. The gelatinous material was taken up in 75 ml water, the aqueous phase extracted with 300 ml portions of ether (3x), the combined organic extracts were backwashed (50 cc H2O), dried (MgSO4), and concentrated (water aspirator) to a crude residue and distilled, b.p. 130°-5° (0.04 mm) to give 35 g (29%) dimethyl 2-oxo-2-phenylethylphosphonate (2a).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04243595 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-4b59926ac9f946be84dceb54d7de561d |
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| Source note | uspto-grants-1981_01 |
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