HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445705Generated: October 30, 2026
Methanesulfonic Acid → Dimethyl (3-oxo-1,3-dihydro-2-benzofuran-1-yl)phosphonate
https://huagongshe.com/reaction/1445705
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Phthalaldehydic acid | HCID 8406 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Dimethylphosphite | HCID 21884954 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Dimethyl (3-oxo-1,3-dihydro-2-benzofuran-1-yl)phosphonate | HCID 11118213 | 132.1% |
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, extracted with chloroform (3×100 ml). The combined organic extracts was washed with water (2×100 ml), dried over MgSO4, and evaporated in vacuo to yield (i) as a white solid (32.0 g, 95%, 95% purity). This was then used without further purification in the next stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07666870B2 |
|---|
| Source dataset | uspto-grants-2010_02 |
|---|
| ORD ID | ord-1730caf19e844a299d4b574c8aad7632 |
|---|
| Source note | uspto-grants-2010_02 |
|---|