HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 360821Generated: October 28, 2026
1,2-Diallyloxybenzene → 3,6-Bis(prop-2-enyl)benzene-1,2-diol
https://huagongshe.com/reaction/360821
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Diallyloxybenzene | HCID 77894 | — |
| Solvent | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Solvent | HCID 87521027 | HCID 87521027 | — |
| Product | 1,2-Diallyloxybenzene | HCID 77894 | 0.77% |
| Product | 3,4-Diallylbenzene-1,2-diol | HCID 13158325 | 13.406% |
| Product | 3,6-Bis(prop-2-enyl)benzene-1,2-diol | HCID 13227678 | 28.082% |
| Internal standard | Ethylbenzene | HCID 7500 | — |
Reaction Conditions
| Temperature | 191.94482421875 °C |
|---|
Reaction carried out in transient flow with ramps to vary the binary solvent composition, temperature and residence time. This reaction represents a single HPLC measurement sampled from within a transient flow ramp. Conditions are an estimate of what the reaction sample was exposed to prior to analysis.
Provenance & Evidence
| DOI | 10.48550/arXiv.2506.07619 |
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| Source dataset | Transient flow exploration of the effect of temperature, residence time and binary solvent ratios on a uni-molecular allyl substituted catechol reaction. |
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| ORD ID | ord-e3e3ff50e9304b90a7a6481c16fc5717 |
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| Source note | Transient flow exploration of the effect of temperature, residence time and binary solvent ratios on a uni-molecular allyl substituted catechol reaction. |
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