HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867792Generated: October 29, 2026
Dimethyl methylphosphonate → HCID 14302187, compound
https://huagongshe.com/reaction/867792
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Benzoic acid, 3-fluoro-, methyl ester | HCID 521184 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14302187 | HCID 14302187 | 83.8% |
Reaction Steps
To a stirred solution of dimethyl methylphosphonate (10.1 g, 81.2 mmol) in 100 ml of anhydrous THF was added dropwise n-butyl lithium (1.58N, 51.4 ml, 81.2 mmol) at -78° C. under argon atmosphere. After 30 minutes, methyl m-fluorobenzoate (5.0 g, 32 mmol) was further added dropwise and the mixture was stirred for 30 minutes. The reaction solution was allowed to warm to 0° C., diluted with 4.9 ml of acetic acid and 10 ml of water, and concentrated. 30 ml of water was added to the residue and the mixture was extracted with ethyl acetate (50 ml×2). The combined ethyl acetate layers were washed with water (20 ml×1) and brine (20 ml×1), dried over anhydrous sodium sulfate, and concentrated. The residue was distilled under reduced pressure to give an oil of dimethyl 2-m-fluorophenyl-2-oxo-ethylphosphonate (6.6 g, 26.8 mmol, yield 83.8%, b.p. 132°-134° C./0.17 mmHg), which was assigned the structure by the following data:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04775692 |
|---|
| Source dataset | uspto-grants-1988_10 |
|---|
| ORD ID | ord-619b735a33c441c085d68bd7d074b4a7 |
|---|
| Source note | uspto-grants-1988_10 |
|---|