HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247679Generated: October 29, 2026
Chlorosuccinimide → N-Hydroxy-4-isobutylbenzenecarboximidoyl chloride
https://huagongshe.com/reaction/2247679
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 4-Isobutylbenzaldehyde oxime | HCID 80256964 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-Hydroxy-4-isobutylbenzenecarboximidoyl chloride | HCID 86620220 | 515.3% |
Reaction Steps
To a solution of 4-isobutylbenzaldehyde oxime (1.0 g, 5.6 mmol) that was obtained in Example 9 (9e) in N,N-dimethylformamide (10 ml) was added N-chlorosuccinimide (0.15 g, 1.1 mmol) with stirring, and furthermore, a small amount of gaseous hydrochloric acid was bubbled into the resulting mixture under stirring, and then the resulting mixture was stirred at room temperature for 10 minutes. After repeating the series of the same procedures described above five times in total, the reaction mixture was poured into ice water (100 ml) and extracted with ether. The extract was washed successively with water and a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. After filtration, the filtrate was evaporated in vacuo to afford the title compound (1.2 g) in a yield of 100% as a yellow oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687491B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-27d681d9ca584b608e8c985b92411b3f |
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| Source note | uspto-grants-2010_03 |
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