HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 360820Generated: October 29, 2026
1,2-Diallyloxybenzene → 3,6-Bis(prop-2-enyl)benzene-1,2-diol
https://huagongshe.com/reaction/360820
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 | 20.328% |
| Product | 3,4-Diallylbenzene-1,2-diol | HCID 13158325 | 18.837% |
| Product | 3,6-Bis(prop-2-enyl)benzene-1,2-diol | HCID 13227678 | 21.834% |
| Internal standard | Ethylbenzene | HCID 7500 | — |
Reaction Conditions
| Temperature | 184.1846466064453 °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 |
|---|
| 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-9f492844a2a24639a58f53d99f9d3ce6 |
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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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