HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262783Generated: October 26, 2026
CID 406 → Dimethyl-2-oxo-3-phenylpropyl phosphonate
https://huagongshe.com/reaction/262783
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | CID 406 | HCID 406 | — |
| Reactant | Methyl phenylacetate | HCID 7559 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Dimethyl-2-oxo-3-phenylpropyl phosphonate | HCID 12805884 | 29% |
Reaction Steps
A solution of 6.2 g (50 mmoles) dimethyl methylphosphonate (Aldrich) in 125 ml dry tetrahydrofuran was cooled to -78° in a dry nitrogen atmosphere. To the stirred phosphonate solution was added 21 ml of 2.37 M n-butyllithium in hexane solution (Alfa Inorganics, Inc.) dropwise over a period of 18 minutes at such a rate that the reaction temperature never rose above -65°. After an additional 5 minutes stirring at -78°, 7.5 g (50.0 mmole) methyl phenylacetate was added dropwise at a rate that kept the reaction temperature less than -70° (20 minutes). After 3.5 hours at -78° the reaction mixture was allowed to warm to ambient temperature, neutralized with 6 ml acetic acid and rotary evaporated to a white gel. The gelatonous material was taken up in 75 ml water, the aqueous phase extracted with 100 ml portions of chloroform (3x), the combined organic extracts were backwashed (50 cc H2O), dried (MgSO4), and concentrated (water aspirator) to a crude residue and distilled, b.p. 134°-5° (<0.1 mm) to give 3.5 g (29%) dimethyl 2-oxo-3-phenylpropylphosphonate. (2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04154949 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-6befe40b9b7b4ba6833581ef4187cd3e |
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| Source note | uspto-grants-1979_05 |
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