HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232173Generated: October 27, 2026
Sodium Iodide → 1-Phthalimido-4-p-toluenesulfonyl-6,6-difluoro-8-benzyloxy-4-aza-octane
https://huagongshe.com/reaction/232173
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | N-3-Bromopropylphthalimide | HCID 21611 | — |
| Reactant | N-(4-benzyloxy-2,2-difluorobutyl)-p-toluenesulfonamide | HCID 19860703 | — |
| Reactant | Potassium tertbutoxide | HCID 50987170 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 1-Phthalimido-4-p-toluenesulfonyl-6,6-difluoro-8-benzyloxy-4-aza-octane | HCID 19860707 | — |
Reaction Steps
To a solution of N-(4-benzyloxy-2,2-difluorobutyl)-p-toluenesulfonamide (7.0 g, 19 mM) in dry DMF (20 mL), is added potassium-tert.-butoxide (2.34 g, 21 mmoles), and the mixture is stirred for 30 minutes. To this mixture are added N-3-bromopropyl-phthalimide (5.1 g, 19 mmoles) and sodium iodide (0.33 g), and the entire mixture is then stirred overnight under nitrogen at room temperature. Following the addition of brine, the mixture is extracted with ether, washed with 1N HCl (twice), then with brine (twice), and dried over Na2SO4. Evaporation of the solvent yields 1-phthalimido-4-p-toluenesulfonyl-6,6-difluoro-8-benzyloxy-4-aza-octane as an oil, which crystallizes on scratching with ether/petroleum ether to form white crystals: 9.5 g (90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04851448 |
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| Source dataset | uspto-grants-1989_07 |
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| ORD ID | ord-ad7a92357fe14e3c9023ec6aea014f51 |
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| Source note | uspto-grants-1989_07 |
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