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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569640Generated: October 30, 2026

Dimethyl methylphosphonate → Dimethyl 2-oxo-4-(3,4-dimethoxyphenyl)butylphosphonate

https://huagongshe.com/reaction/569640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl methylphosphonateHCID 12958—
ReactantMethyl 3-(3,4-dimethoxyphenyl)propanoateHCID 520347—
ReactantButyllithiumHCID 178418339—
SolventSodium ChlorideHCID 5234—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductDimethyl 2-oxo-4-(3,4-dimethoxyphenyl)butylphosphonateHCID 2014793628.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a mixture cooled at -78° C. of 50 ml of 2.1M n-butyl lithium solution in hexane and 100 ml of tetrahydrofuran, was added dropwise 12.4 g of dimethyl methylphosphonate. The mixture was stirred at -78° C. for 30 minutes, and thereafter 22.4 g of methyl 3-(3,4-dimethoxyphenyl)propionate [synthesized from 3,4-dimethoxycinnamic acid in 2 steps: (a) esterification (HCl--CH3OH) and (b) reduction (Pd/C--H2)] and 100 ml of tetrahydrofuran were added dropwise to the mixture. Then, the reaction was continued at -78° C. for 22 hours. The reaction mixture was poured in 500 ml of saturated aqueous sodium chloride solution. After neutralization and extraction with dichloromethane, the extract was dried and concentrated to give crude product. By purification of the crude product by means of column chromatography (silica gel/hexane:ethyl acetate=1:4), 9.0 g of the above caption compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04733002
Source datasetuspto-grants-1988_03
ORD IDord-8709608733304e8d8035a1795b7ee7de
Source noteuspto-grants-1988_03