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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289192Generated: October 30, 2026

Hydrochloric Acid → dimethyl (S)-hydroxy(p-methylphenyl)methylphosphonate

https://huagongshe.com/reaction/2289192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-MethylbenzaldehydeHCID 7725—
ReactantDimethylphosphiteHCID 21884954—
Productdimethyl (S)-hydroxy(p-methylphenyl)methylphosphonateHCID 1077578682%

Reaction Steps

The solution of ALB in tetrahydrofuran (0.1 M, 0.40 ml) obtained in Example 1 was concentrated at room temperature for 1 hour under reduced pressure, then 0.4 ml of toluene was added thereto under an argon atmosphere. To this solution was added dimethyl phosphite (37 μl, 0.40 mmol) at room temperature. After stirring at room temperature for 30 minutes, the reaction vessel was cooled to -40° C., and it was maintained at this temperature for 0.15 minutes. Then p-methylbenzaldehyde (0.40 mmol) was added thereto. After reacting for 92 hours, 1N hydrochloric acid was added thereto to stop the reaction. The mixture was extracted with ethyl acetate (10 ml×three times), and the combined extracts were washed with brine and dried over Na2SO4. The solvent was distilled, and the residue was purified by flash column chromatography (acetone/hexane=1/5, on SiO2) to obtain dimethyl (S)-hydroxy(p-methylphenyl)methylphosphonate as a final product in a yield of 82%. The chemical reaction in this Example is shown in chemical formula 29. ##STR23##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090969
Source datasetuspto-grants-2000_07
ORD IDord-1c99cc3887e54d388922821cf6e3aae6
Source noteuspto-grants-2000_07