HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439253Generated: October 25, 2026
Acetic Acid → Dimethyl (3,3-dimethyl-2-oxo-4-phenylbutyl)phosphonate
https://huagongshe.com/reaction/1439253
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | Dimethyl (3,3-dimethyl-2-oxo-4-phenylbutyl)phosphonate | HCID 14302191 | — |
Reaction Steps
To a solution of 63 g. of dimethylmethylphosphonate in 600 ml. of tetrahydrofuran under nitrogen at -75° C. is added with stirring 312 ml. of 1.6 molar n-butyllithium in hexane. The addition rate is adjusted so that the reaction temperature remains below 55° C. Ten minutes after the addition is complete, 48.2 g. of the reaction product of part B of this example and 50 ml. of tetrahydrofuran are added dropwise at such rate as to maintain the reaction temperature below -60° C. The resulting mixture is then stirred at -75° C. for 2 hours and then ambient temperature overnight. Acetic acid (20 ml.) is thereafter added and the resulting mixture distilled under vacuum, thereby removing most of the tetrahydrofuran. The residue is then shaken with diethyl ether in methylene chloride (3:1 by volume) and a cold dilute sodium bicarbonate solution. The organic layer is then washed with brine, dried, and concentrated. The residue is crystallized from diethyl ether, yielding 54 g. of dimethyl 3,3-dimethyl-2-oxo-4-phenylbutylphosphorate the title compound. The melting point is 48°-50° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04058564 |
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| Source dataset | uspto-grants-1977_11 |
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| ORD ID | ord-1087e653294a45588957fc8cba9981f6 |
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| Source note | uspto-grants-1977_11 |
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