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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528513Generated: October 26, 2026

Trifluoroacetic acid → (Hydroxy-(3,4,5-trimethoxy-phenyl)-methyl]-phosphonic acid dimethyl ester

https://huagongshe.com/reaction/1528513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant3,4,5-TrimethoxybenzaldehydeHCID 6858—
ReactantDimethyl phosphate anionHCID 3753418—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product(Hydroxy-(3,4,5-trimethoxy-phenyl)-methyl]-phosphonic acid dimethyl esterHCID 1410168788%

Reaction Conditions

Temperature0 °C

Reaction Steps

A round-bottom flask equipped with thermometer, condenser and gas inlet was charged with methanol (150 mL) and sodium methoxide (1.074 g, 20 mmol) and cooled to 0° C. under nitrogen protection. To a stirred solution were added subsequently dimethyl phosphate (19.52 g, 0.177 mol) and 3,4,5-trimethoxybenzaldehyde (30 g, 0.153 mol). A resulted solution was heated at 50° C. for 1 hour, cooled down to r.t. and treated with trifluoroacetic acid (4.6 ml). The mixture was concentrated under reduced pressure, the residue dissolved in EtOAc (300 mL), washed once with 18% brine, then once with saturated brine, dried over sodium sulfate. The filtered solution was concentrated until precipitation started. To the resulted suspension 1:1 mixture of t-butylmethyl ether and heptane was added (50 mL). Solid was filtered out, washed with two portions (20 mL) of the same solvent mixture and vacuum-dried to give 41.2 g (88%) of 1, LC purity 99.4% (AUC), m.p. 103-104° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090603B2
Source datasetuspto-grants-2015_07
ORD IDord-c3c7108e2a6a418b9451c418b4763fb0
Source noteuspto-grants-2015_07