HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970864Generated: October 30, 2026
Triethylamine → 2-(cyclohexylmethoxy)-1H-isoindole-1,3(2H)-dione
https://huagongshe.com/reaction/970864
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | Cyclohexane, (bromomethyl)- | HCID 137636 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(cyclohexylmethoxy)-1H-isoindole-1,3(2H)-dione | HCID 14074416 | 53% |
Reaction Steps
To a stirred solution of N-hydroxyphthalimide (10.0 g, 61.30 mmol) in DMF (40 mL) at RT was added NEt3 (9.40 mL, 67.43 mmol) and, in a dropwise fashion, (bromomethyl)cyclohexane (9.41 mL, 67.43 mmol). The reaction was then stirred for 15 hours at 50° C., after which it was allowed to cool to RT and then concentrated under vacuum. The residue was dissolved in Et2O (100 mL) and washed with water, brine, dried over MgSO4 and the solvent removed under reduced pressure. The residue was purified by column chromatography (eluting with CH2Cl2/PE, 1:1 to 3:1) to afford N-(cyclohexylmethoxy)phthalimide (8.40 g, 53%), as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07312248B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-4f03575b0c2a4e62814cb4120aef2577 |
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| Source note | uspto-grants-2007_12 |
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