Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 14579490 | HCID 14579490 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 14231038 | HCID 14231038 | — |
Reaction Steps
A mixture of 2-fluoromethyl-2-phthalimido-6-iodohexanenitrile (9.0 g, 22.5 mmol), dry DMF (30 ml), and potassium phthalimide (4.2 g, 1 equivalent) is stirred and heated at 80° C. for 4 hours. The DMF is removed under reduced pressure (0.1 mm Hg), and the residue is taken up in chloroform. The chloroform mixture is filtered and the filtrate is washed with 2N NaOH, 2N HCl, and water. Evaporation of solvent gives a residue which, when dissolved in the minimum amount of acetone, crystallizes upon addition of ether. After standing at 5° C. overnight, the colourless crystals of 2-fluoromethyl-2,6-diphthalimidohexanenitrile are collected (7.0 g), m.p. (Kofler) 136° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04866206 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-76130c3f73ef43f19524f75aa5c6a4eb |
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| Source note | uspto-grants-1989_09 |
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