Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267461Generated: October 30, 2026

Acetic Acid → Dimethyl (2-oxo-3-(3-(trifluoromethyl)phenyl)propyl)-phosphonate

https://huagongshe.com/reaction/1267461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantN-methoxy-N-methyl-2-[3-(trifluoromethyl)phenyl]acetamideHCID 22712418—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductDimethyl (2-oxo-3-(3-(trifluoromethyl)phenyl)propyl)-phosphonateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552067B2
Source datasetuspto-grants-2003_04
ORD IDord-a115ff82cb3141a785d6f9df9d41d8c3
Source noteuspto-grants-2003_04