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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13917Generated: October 30, 2026

Benzyl Bromide → HCID 68583816, compound

https://huagongshe.com/reaction/13917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Prop-2-en-1-yl)-5,6,7,8-tetrahydronaphthalen-1-olHCID 68583287—
CatalystTetrabutylammonium IodideHCID 67553—
ProductHCID 68583816HCID 6858381688.2%

Reaction Steps

Treatment of 2-allyl-5,6,7,8-tetrahydronaphthalen-1-ol (18.48 g, 0.098 mol) with potassium carbonate (41.46 g, 0.300 mol), benzyl bromide (18.81 g, 0.110 mol), and tetrabutylammonium iodide (7.39 g, 0.020 mol) generally according to the procedure described for Intermediate 1 afforded 24.05 g (88%) of 2-allyl-5,6,7,8-tetrahydronaphthalen-1-yl benzyl ether as a pale yellow oil. Rf=0.39 (silica, ethyl acetate:hexanes 1:19); Anal. calcd. for C20H22O0.2H2O: C, 85.19; H, 8.01. Found: C, 84.95; H, 7.75.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728155B2
Source datasetuspto-grants-2010_06
ORD IDord-4af40855a52e4385bf6d7111eeefc971
Source noteuspto-grants-2010_06