HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222002Generated: October 28, 2026
N-Carbethoxyphthalimide → 2-(2-(4-Bromophenyl)-5,8-dioxaspiro[3.4]octan-2-yl)isoindoline-1,3-dione
https://huagongshe.com/reaction/222002
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Carbethoxyphthalimide | HCID 31187 | — |
| Reactant | 2-(4-Bromophenyl)-5,8-dioxaspiro[3.4]octan-2-amine | HCID 58216602 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(2-(4-Bromophenyl)-5,8-dioxaspiro[3.4]octan-2-yl)isoindoline-1,3-dione | HCID 58216606 | — |
Reaction Steps
A mixture of 2-(4-bromophenyl)-5,8-dioxaspiro[3.4]octan-2-amine (7-1) (2.7 g, 9.50 mmol), ethyl 1,3-dioxo-1,3-dihydro-2H-isoindole-2-carboxylate (4.2 g, 19.0 mmol), and TEA (5.3 mL, 38.0 mmol) in CHCl3 (50 mL) was stirred at 70° C. for overnight. The solvent was evaporated under reduced pressure, and to the residue was added MeOH. The resulting solid was collected by filtration to give 2-[2-(4-bromophenyl)-5,8-dioxaspiro[3.4]oct-2-yl]-1H-isoindole-1,3(2H)-dione (7-2) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207169B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-a288a75db540489bb30c9030d98da4ef |
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| Source note | uspto-grants-2012_06 |
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