HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422875Generated: November 2, 2026
Azobisisobutyronitrile → HCID 86726295, compound
https://huagongshe.com/reaction/1422875
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Cyclohexene | HCID 8079 | — |
| Reactant | HCID 86726294 | HCID 86726294 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86726295 | HCID 86726295 | 81% |
Reaction Steps
To a stirred solution of ((S)-1-phenylcarbamoyl-hex-5-enyl)-carbamic acid tert-butyl ester (250 mg, 0.78 mmol), thioacetic acid (564 μl, 7.8 mmol) at 75° C. in degassed dioxane was added AIBN (129 mg, 0.78 mmol). The reaction mixture was stirred for 1 hour. The reaction mixture was cooled to 0° C. and an excess of cyclohexene was added under stirring, the latter being maintained for 20 mn. The reaction mixture was concentrated under reduced pressure, and the resulting crude product was rinsed more times with hexane to afford the desired adduct.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927533B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-f06a9510870f4162814391997e868339 |
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| Source note | uspto-grants-2015_01 |
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