HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741325Generated: November 1, 2026
p-Toluenesulfonic acid monohydrate → HCID 10679822, compound
https://huagongshe.com/reaction/1741325
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 21834061 | HCID 21834061 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 10679822 | HCID 10679822 | — |
Reaction Steps
0.56 g of p-toluenesulfonic acid monohydrate was added to a solution of 8.62 g of N-[2-(tetrahydropyran-2-yloxy)ethoxy]phthalimide [prepared as described in step (a) above] in 86 ml of methanol, and the resulting mixture was stirred at room temperature for 2 hours. At the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure, and then the resulting residue was dissolved in a mixture of ethyl acetate and water and neutralyzed with sodium hydrogen carbonate. The ethyl acetate layer was separated and-dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure, giving the title compound as a crystalline powder. This was washed with diisopropyl ether to give 4.10 g of the pure compound, melting at 82-85° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05972959 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-47ca880867f54af08135d830ca041894 |
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| Source note | uspto-grants-1999_10 |
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