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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 360608Generated: October 28, 2026

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

https://huagongshe.com/reaction/360608

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DiallyloxybenzeneHCID 77894—
SolventAcetonitrileHCID 6342—
SolventAcetonitrile aceticacidHCID 22391770—
Product1,2-DiallyloxybenzeneHCID 778940%
Product3,4-Diallylbenzene-1,2-diolHCID 131583251.94%
Product3,6-Bis(prop-2-enyl)benzene-1,2-diolHCID 132276781.144%
Internal standardEthylbenzeneHCID 7500—

Reaction Conditions

Temperature225 °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-1507484e59c44891913e8ebf32c83ce7
Source noteTransient flow exploration of the effect of temperature, residence time and binary solvent ratios on a uni-molecular allyl substituted catechol reaction.