HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481329Generated: October 31, 2026
Phthalimide → 2-(2-Bromo-4,6-dichlorobenzyl)isoindoline-1,3-dione
https://huagongshe.com/reaction/1481329
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-Bromo-2-(bromomethyl)-3,5-dichlorobenzene | HCID 10426068 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(2-Bromo-4,6-dichlorobenzyl)isoindoline-1,3-dione | HCID 89704758 | — |
Reaction Steps
To a solution of 1-bromo-2-(bromomethyl)-3,5-dichlorobenzene (1.98 mmol) [J. Med. Chem., 35 (22), 4221 (1992)] in 10 mL CH3CN were added phthalimide (1.98 mmol) and K2CO3 (5.93 mmol). The reaction mixture was stirred at 50° C. for 6 h and then at RT overnight. Sat. aq. NaHCO3 solution was added and the mixture was extracted 3 times with DCM. The combined organic phases were dried over MgSO4 and concentrated in vacuo to obtain the desired product as beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409917B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-a933f82de4ac4c0abdc229076866e97c |
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| Source note | uspto-grants-2016_08 |
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