HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436076Generated: October 30, 2026
Azobisisobutyronitrile → HCID 24784534, compound
https://huagongshe.com/reaction/1436076
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-Bromosuccinamide | HCID 9834204 | — |
| Reactant | HCID 24784533 | HCID 24784533 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 24784534 | HCID 24784534 | 54.1% |
Reaction Steps
2-(4,4-Dimethyl-2-oxo-1,3-oxazolidin-3-yl)-4,5-dihydronaphtho[1,2-d][1,3]thiazole-7-carbonitrile (0.65 g, 2.0 mmol), prepared in step 5 of Example 6, N-bromosuccinamide (0.39 g, 2.2 mmol) and a catalytic amount of 2,2′-azobis(2-methylproprionitrile) were stirred in carbontetrachloride (68 mL) at reflux for 4 h. The reaction was diluted with ethyl acetate and washed with 10% sodium thiosulfate. The layers were separated and the organic layer was dried over anhydrous MgSO4, filtered and concentrated to give 0.64 g of crude product. Purification of the crude product on silica gel using a stepwise gradient of 6:1 to 1:1 hexane:ethyl acetate as the eluent gave 0.35 g of product that contained an impurity. Recrystallization from ethyl acetate afforded the title compound (0.02 g, 3%), mp>230° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07618989B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-b10525d77d994e0d9d2c08d5103cd55e |
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| Source note | uspto-grants-2009_11 |
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