HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256392Generated: November 2, 2026
Phthalic Anhydride → N-(5-Bromopentyl)phthalimide
https://huagongshe.com/reaction/2256392
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 5-Aminopentan-1-ol | HCID 75634 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(5-Bromopentyl)phthalimide | HCID 136770 | 70% |
Reaction Steps
To a suspension n of phthalic anhydride (2.96 g, 20 mmol) in toluene (20 mL) was added 5-amino-1-pentanol (2.2 mL, 20 mmol) and the resulting mixture was heated to reflux for 14 hours. The solvent was removed under reduced pressure and the residue dissolved in dichloromethane (20 mL). This solution was cooled to 0° C. and triphenylphosphine (4.7 g, 18 mmol) and bromine were added. After warming to room temperature, the solution was stirred overnight and then poured into water (20 mL) and the organic phase was separated. The aqueous phase was extracted with dichloromethane (20 mL) and the combined organic phases were dried over sodium sulfate and evaporated to dryness. Silica gel chromatography using hexane/ethyl acetate (4:1) as the eluent gave the title compound as a syrup (4.13 g, 70% for 2 steps).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05654431 |
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| Source dataset | uspto-grants-1997_08 |
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| ORD ID | ord-a6ca028a56294012909a1f754d581dd4 |
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| Source note | uspto-grants-1997_08 |
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