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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTetrahydrofuranHCID 8028—
ReactantHexaneHCID 8058—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantButyllithiumHCID 178418339—
ProductDimethyl (3,3-dimethyl-2-oxo-4-phenylbutyl)phosphonateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04058564
Source datasetuspto-grants-1977_11
ORD IDord-1087e653294a45588957fc8cba9981f6
Source noteuspto-grants-1977_11