HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925225Generated: October 30, 2026
N-bromobutanimide → HCID 86725335, compound
https://huagongshe.com/reaction/925225
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 59730230 | HCID 59730230 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86725335 | HCID 86725335 | 68.4% |
Reaction Steps
Into a 100 ml flask, the product of step (d) (1.65 g, 6.37 mmol) dissolved in acetonitrile (25 ml) was added. To this stirred solution, NBS (1.07 g, 6.05 mmol) was added. The reaction mixture was heated to 80° C. for 15 minutes and then partitioned between water and EtOAc. The aqueous layer was extracted with EtOAc (3×). The combined EtOAc extracts were washed with brine, dried over Na2SO4, and solvent evaporated in vacuo to give the crude product. Purification by silica-gel chromatography (gradient elution: 0 to 40% EtOAc in hexanes) gave the sub-title compound as a yellow solid (1.4 g). MS: ESI (positive): 338, 340 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284277B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-d4e5eb3ed0684e538a84a2e29ba1ad15 |
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| Source note | uspto-grants-2016_03 |
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