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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466736Generated: October 27, 2026

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

https://huagongshe.com/reaction/1466736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantPhthalaldehydic acidHCID 8406—
ReactantDimethyl ester phosphorous acidHCID 94853—
ReactantSodiumHCID 5360545—
SolventMethanolHCID 887—
ProductDimethyl (3-oxo-1,3-dihydro-2-benzofuran-1-yl)phosphonateHCID 1111821367.3%

Reaction Steps

To dry methanol (40 ml) was slowly added sodium (1.15 g, 50 mmol) at 0 under N2 atmosphere while stirring, then added dimethyl hydrogen phosphite (5.5 g, 50 mmol), and 2-formylbenzoic acid (5.25 g, 35 mmol). The ice bath was removed and the reaction mixture was stirred for 30 min at room temperature, and then the reaction mixture was slowly added methanesulfonic acid (5.5 g, 55 mmol) and concentrated at reduced pressure to give the crude residue. The crude residue was partitioned between DCM and cold water (100 ml each), and the organic phase was washed with water and brine, dried over sodium sulphate, filtered, and concentrated to give the crude product (5.7 g, 67%) as an off white solid, used in next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999985B2
Source datasetuspto-grants-2015_04
ORD IDord-a3ab18e4471645d0a8bbf30424b95826
Source noteuspto-grants-2015_04