HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249503Generated: October 31, 2026
Dimethylformamide → HCID 178514998, compound
https://huagongshe.com/reaction/1249503
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-3-Bromopropylphthalimide | HCID 21611 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178514998 | HCID 178514998 | — |
Reaction Steps
N-(3-Bromopropyl)phthalimide (164 g) is added to a stirred solution of 5-hydroxy-1,2-dihydro-1-(2H)-isoquinolone (96.7 g) and anhydrous K2CO3 (91.2 g) in 750 ml of DMF. The reaction mixture is stirred at room temperature for one week, diluted with 3 liters of H2O and stirring continued at RT for an additional 30 minutes. The reaction mixture is filtered and the solid resuspended in 2 liters of H2O and stirred at RT for an additional 11/2 hours. The suspension is filtered and the solid dried in air. The dried solid is broken up, suspended in 750 ml of chloroform and stirred vigorously at RT for 1 hour. The suspension is filtered and the solid dried. The crude product (95.8 g) is dissolved in 2.5 liters in boiling glacial acetic acid. The resulting dark solution is concentrated and cooled. The crystalline precipitate is collected and dried, washed with diethyl ether, resuspended in diethyl ether, stirred at RT for 30 minutes, filtered and dried in vacuo overnight, yielding 59.3 g of the desired product, M.P.>300° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04632927 |
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| Source dataset | uspto-grants-1986_12 |
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| ORD ID | ord-d536e5a6bed04bcda2728ba4934f19ac |
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| Source note | uspto-grants-1986_12 |
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