Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361060Generated: October 31, 2026

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

https://huagongshe.com/reaction/361060

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DiallyloxybenzeneHCID 77894—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product1,2-DiallyloxybenzeneHCID 7789414.462%
Product3,4-Diallylbenzene-1,2-diolHCID 1315832528.31%
Product3,6-Bis(prop-2-enyl)benzene-1,2-diolHCID 1322767825.896%
Internal standardEthylbenzeneHCID 7500—

Reaction Conditions

Temperature209.0662384033203 °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-99bd9fd487a04474ac32ef527f404375
Source noteTransient flow exploration of the effect of temperature, residence time and binary solvent ratios on a uni-molecular allyl substituted catechol reaction.