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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Methyl 3-(3,4-dimethoxyphenyl)propanoate | HCID 520347 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Sodium Chloride | HCID 5234 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Dimethyl 2-oxo-4-(3,4-dimethoxyphenyl)butylphosphonate | HCID 20147936 | 28.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04733002 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-8709608733304e8d8035a1795b7ee7de |
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| Source note | uspto-grants-1988_03 |
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