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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 360213Generated: October 29, 2026

1,2-Diallyloxybenzene → 3,4-Diallylbenzene-1,2-diol

https://huagongshe.com/reaction/360213

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DiallyloxybenzeneHCID 77894—
Solvent2-MethyltetrahydrofuranHCID 7301—
Solvent1,1,1,3,3,3-Hexafluoro-2-propanolHCID 13529—
Product1,2-DiallyloxybenzeneHCID 7789433.32%
Product3,4-Diallylbenzene-1,2-diolHCID 1315832534.29%
Product3,6-Bis(prop-2-enyl)benzene-1,2-diolHCID 1322767827.489%
Internal standardEthylbenzeneHCID 7500—

Reaction Conditions

Temperature175 °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

DOI10.48550/arXiv.2506.07619
Source datasetTransient flow exploration of the effect of temperature, residence time and binary solvent ratios on a uni-molecular allyl substituted catechol reaction.
ORD IDord-cc7c3502d722438d9af9c8b9d8c77ea9
Source noteTransient flow exploration of the effect of temperature, residence time and binary solvent ratios on a uni-molecular allyl substituted catechol reaction.