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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115935Generated: November 1, 2026

Guaiacol → HCID 10967048, compound

https://huagongshe.com/reaction/2115935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuaiacolHCID 460—
ReactantPhenolHCID 996—
ReactantBenzyl BromideHCID 7498—
ReactantAllyl bromideHCID 7841—
ReactantDiallyl etherHCID 11194—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methoxy-6-(prop-2-en-1-yl)phenolHCID 347577—
CatalystTetrabutylammonium IodideHCID 67553—
Solventtert-ButanolHCID 6386—
SolventMesityleneHCID 7947—
ProductHCID 10967048HCID 1096704845%

Reaction Steps

Treatment of guaiacol (25.00 g, 0.201 mol) with allyl bromide (29.24 g, 0.242 mol) and potassium carbonate (83.50 g, 0.604 mol) followed by refluxing the resultant allyl ether in mesitylene generally according to the procedure described for Intermediate 8 afforded 2-allyl-6-methoxyphenol as a brown oil. Treatment of the phenol with potassium carbonate (83.5 g, 0.604 mol), benzyl bromide (36.19 g, 0.212 mol), and tetrabutylammonium iodide (7.42 g, 0.020 mol) generally according to the procedure described for Intermediate 1 gave 23.61 g (45%) of 1-allyl-2-(benzyloxy)-3-methoxybenzene as a pale yellow oil. Rf=0.71 (silica, ethyl acetate:hexanes 1:9); Anal. calcd. for C17H18O2: C, 80.28; H, 7.13. Found: C, 79.09; H, 6.93.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435837B2
Source datasetuspto-grants-2008_10
ORD IDord-2635616f4f0c46fb922d7ccf270fe0c7
Source noteuspto-grants-2008_10