Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phthaloyl chloride | HCID 6955 | — |
| Reactant | 4-Fluorobenzylamine | HCID 67326 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 1000719 | HCID 1000719 | 82% |
Reaction Steps
To a mixture of phthaloyl dichloride (3 g, 15 mmol, 1 eq) in toluene (HPLC grade, 20 mL), cooled to 0° C., was added slowly a solution of 4-fluorobenzylamine (4.62 g, 37 mmol, 2.2 eq) in toluene (5 mL). After stirring at ambient temperature for 24 h, the reaction mixture was concentrated in vacuo to remove toluene. The resultant residue was dissolved in DCM, washed with brine and dried over Na2SO4. The organic layer was evaporated under reduced pressure. Recrystallization from DCM:hexane afforded the desired compound (4.6 g, 82%). 1H NMR (400 MHz, DMSO-d6) δ 9.3 (s, 2H), 9.1 (s, 2H), 8.64 (s, 1H), 7.39-7.34 (m, 4H), 7.17-7.12 (m, 4H), 4.48-4.46 (d, 4H). MS (ESI): 381.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501992B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-36b2448684f84ea9964bdd05a6bd1535 |
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| Source note | uspto-grants-2013_08 |
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