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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Methylbenzaldehyde | HCID 7725 | — |
| Reactant | Dimethylphosphite | HCID 21884954 | — |
| Product | dimethyl (S)-hydroxy(p-methylphenyl)methylphosphonate | HCID 10775786 | 82% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06090969 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-1c99cc3887e54d388922821cf6e3aae6 |
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| Source note | uspto-grants-2000_07 |
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