HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649981Generated: November 2, 2026
HCID 13674813, compound → HCID 13674820, compound
https://huagongshe.com/reaction/1649981
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 13674813 | HCID 13674813 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13674820 | HCID 13674820 | 64.1% |
Reaction Steps
33.3 g/0.19 moles of potassium phthalimide are added to a solution of 30 g (89 mmoles) of 1-[N-(2,6-dimethylphenyl)-methane-sulfonamido]-2-methanesulfonyloxy-propane in 300 ml of dry dimethyl formamide, and the mixture is stirred at 145°-150° C. for one hour. The mixture is cooled, poured onto 800 ml of ice water, and the aqueous mixture is extracted thrice with 200 ml of chloroform, each. The chloroform solution is washed thrice with 50 ml of n sodium hydroxide solution and then thrice with 100 ml of water, each, dried over anhydrous magnesium sulfate, and the solvent is evaporated under reduced pressure. The oily residue is triturated with 35 ml of isopropanol, the separated crystalline substance is filtered off, washed with ice-cold isopropanol and dried. 22 g (64.1%) of 1-[N-(2,6-dimethylphenyl)-methanesulfonamido]-2-phthalimido-propane are obtained as a colourless, crystalline substance; m.p.: 124°-127° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04922021 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-2d2e6996ea2f4306a6975071203b08d4 |
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| Source note | uspto-grants-1990_05 |
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