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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422875Generated: November 2, 2026

Azobisisobutyronitrile → HCID 86726295, compound

https://huagongshe.com/reaction/1422875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantCyclohexeneHCID 8079—
ReactantHCID 86726294HCID 86726294—
ReactantHCID 178418634HCID 178418634—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86726295HCID 8672629581%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927533B2
Source datasetuspto-grants-2015_01
ORD IDord-f06a9510870f4162814391997e868339
Source noteuspto-grants-2015_01