HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600958Generated: October 27, 2026
Cyclohexyl bromide → N-cyclohexyloxyphthalimide
https://huagongshe.com/reaction/600958
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexyl bromide | HCID 7960 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-cyclohexyloxyphthalimide | HCID 10467039 | 93% |
Reaction Steps
Solid potassium carbonate (6.91 g, 50.0 mmol) was added to a solution of N-hydroxyphthalimide (4.08 g, 25.0 mmol) and 18-crown-6 (661 mg, 2.5 mmol) in dimethyl sulfoxide (62 mL), and the mixture was stirred at 25° C. for 5 min. To the mixture cyclohexyl bromide (12.3 mL, 100.0 mmol) was added, and the mixture stirred at 80° C. for 3 h. After ice-cooling, the mixture was poured into cold water and the resulting precipitate was collected by filtration in vacuo, washed with water (25 mL) and hexanes (15 mL) and dried in vacuo to afford 2-cyclohexyloxy-isoindole-1,3-dione (5.67 g, 93%) as a white solid which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902248B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-46185667d80246249f0f6c1bdd70dcd2 |
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| Source note | uspto-grants-2011_03 |
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