HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247445Generated: October 25, 2026
Sodium Carbonate → 4-(4-Aminophenyl)isoindolin-1-one
https://huagongshe.com/reaction/1247445
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline | HCID 2734620 | — |
| Reactant | 4-Bromoisoindolin-1-one | HCID 21907509 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 4-(4-Aminophenyl)isoindolin-1-one | HCID 21907511 | 59.1% |
Reaction Steps
A suspension of Example 1C (2 g, 9.43 mmol), 4-(4,4,5,5-tetramethyl-1,3,2-dioxa-borolan-2-yl)aniline (2.5 g, 11.3 mmol), and Na2CO3 (2.2 g, 20.8 mmol) in DME (68 mL) and water (17 mL) was purged with nitrogen, treated with Pd(PPh3)4 (1 g, 0.9 mmol), and stirred at 90° C. for 19 hours. The reaction mixture was cooled to room temperature, concentrated to one-third its original volume, diluted with ethyl acetate (30 mL) and water (20 mL), and filtered. The filter cake was washed with water and ethyl acetate and dried to give 1.25 g of the desired product. MS (ESI(+)) m/e 225 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129260B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-87b529d2005243cfbdf445e422b4fe49 |
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| Source note | uspto-grants-2006_10 |
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