HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459001Generated: October 30, 2026
Acetic Acid → Dimethyl (2-oxo-3-(3-(trifluoromethyl)phenyl)propyl)-phosphonate
https://huagongshe.com/reaction/459001
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | N-methoxy-N-methyl-2-[3-(trifluoromethyl)phenyl]acetamide | HCID 22712418 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Dimethyl (2-oxo-3-(3-(trifluoromethyl)phenyl)propyl)-phosphonate | HCID 17781240 | — |
Reaction Steps
To a solution of dimethyl methylphosphonate (9.4 g, 75.8 mmol) in toluene (80 mL) at −78° C. was slowly added n-BuLi (2.5M in hexanes, 28 mL, 70 mmol). The reaction mixture was stirred for 1 h and a solution of N-methoxy-N-methyl-2-(3-trifluoromethyl-phenyl)-acetamide (14.39 g) in toluene (50 mL) was slowly added. The reaction mixture was stirred for 2.5 h and AcOH (40 mL) was added. The reaction mixture was warmed to room temperature and water was added. The organic layer was washed with water followed by brine. The organic solution was dried (MgSO4), filtered and concentrated in vacuo. Medium pressure chromatography (CH2Cl2 to 2% MeOH in CH2Cl2) provided the title compound of Preparation 10 (9.37 g). 1H NMR (CDCl3) δ7.52 (m, 1H), 7.44 (m, 2H), 7.37 (m, 1H), 3.96 (s, 2H), 3.87 (s, 3H), 3.76 (s, 3H), 3.12 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07192979B2 |
|---|
| Source dataset | uspto-grants-2007_03 |
|---|
| ORD ID | ord-53ea7163ab0045a1badaa937f06da484 |
|---|
| Source note | uspto-grants-2007_03 |
|---|