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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269964Generated: October 26, 2026

Methanesulfonic Acid → Dimethyl (3-oxo-1,3-dihydro-2-benzofuran-1-yl)phosphonate

https://huagongshe.com/reaction/269964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantPhthalaldehydic acidHCID 8406—
ReactantSodium MethoxideHCID 10942334—
ReactantDimethylphosphiteHCID 21884954—
SolventMethanolHCID 887—
ProductDimethyl (3-oxo-1,3-dihydro-2-benzofuran-1-yl)phosphonateHCID 11118213—

Reaction Conditions

Temperature20 °C

Reaction Steps

Dimethyl phosphite (22.0 g, 0.2 mol) was added drop-wise to a solution of sodium methoxide (43.0 g) in methanol (100 ml) at 0° C. 2-Carboxybenzaldehyde (21.0 g, 0.1 mol) was then added portion-wise to the reaction mixture as a slurry in methanol (40 ml), with the temperature kept below 5° C. The resulting pale yellow solution was warmed to 20° C. over 1 hour. Methanesulphonic acid (21.2 g, 0.22 mol) was added to the reaction drop-wise and the resulting white suspension was evaporated in vacuo. The white residue was quenched with water and extracted into chloroform (3×100 ml). The combined organic extracts were washed with water (2×100 ml), dried over MgSO4, and evaporated in vacuo to yield (3-oxo-1,3-dihydro-isobenzofuran-1-yl)phosphonic acid dimethyl ester as a white solid (32.0 g, 95%, 95% purity). This was then used without further purification in the next stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449464B2
Source datasetuspto-grants-2008_11
ORD IDord-6ff759119ac540f0b5fd1dceb834ca69
Source noteuspto-grants-2008_11