HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867755Generated: October 31, 2026
Acetic Acid → Dimethyl (3,3-dimethyl-2-oxopentyl)phosphonate
https://huagongshe.com/reaction/867755
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Methyl 2,2-dimethylbutanoate | HCID 522750 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Dimethyl (3,3-dimethyl-2-oxopentyl)phosphonate | HCID 14302171 | 50% |
Reaction Steps
Dimethyl methylphosphonate (9.3 g, 0.075 mol) was dissolved in anhydrous THF (80 ml) under argon atmosphere. To the solution stirred at -78° C. was added dropwise n-butyl lithium (1.61N, 47 ml, 0.075 mol) over 30 minutes, and then a solution of 2,2-dimethylbutanoic acid methyl ester (3.9 g, 0.03 mol) in anhydrous THF (10 ml) was also added dropwise over 30 minutes. The reaction mixture was warmed to room temperature and stirred for 30 minutes. Under ice cooling, acetic acid (4.5 ml) and water (10 ml) were added to the mixture. After concentration, water (20 ml) was added to the residue, and the mixture was then extracted with ethyl acetate (50 ml×2). The ethyl acetate layers were washed with water (20 ml×1) and with brine (20 ml×1), dried over anhydrous sodium sulfate, and concentrated. Distillation of the residue gave dimethyl 3,3-dimethyl-2-oxo-pentylphosphonate (3.36 g, 0.015 mol, yield: 50%, b.p.=115-117/0.5 mmHg). The structure was identified 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-82749d28a6b649eea42dc385063534db |
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| Source note | uspto-grants-1988_10 |
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