HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639946Generated: October 29, 2026
Dimethyl methylphosphonate → HCID 86620239, compound
https://huagongshe.com/reaction/639946
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | HCID 68420425 | HCID 68420425 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86620239 | HCID 86620239 | — |
Reaction Steps
To a solution of dimethyl methylphosphonate (0.7 mL) in THF (8.2 mL) was added 2.44 M n-butyllithium/n-hexane solution (2.6 mL) at −78° C., and the reaction mixture was stirred for 0.5 hr at −78° C. A solution of [2-benzyloxy-5-(4-ethylbenzyl)benzyl chloride (1.50 g) in THF (8.2 mL) was added to the mixture at −78° C., and the reaction mixture was stirred for 2 hr at −78° C.˜−10° C. The reaction was quenched by the addition of saturated aqueous ammonium chloride and extracted with ethyl acetate. The combined ethyl acetate extracts were washed with brine, dried over anhydrous sodium sulfate and evaporated. The residue was purified by silica gel column chromatography (ethyl acetate/n-hexane=2/3) to give the title compound (0.74 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07691898B2 |
|---|
| Source dataset | uspto-grants-2010_04 |
|---|
| ORD ID | ord-8608e20c4be04f6699dbc7955ed8af53 |
|---|
| Source note | uspto-grants-2010_04 |
|---|