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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373489Generated: October 30, 2026

p-Xylyl bromide → [5-(Benzyloxy)-1-(4-methylbenzyl)-1H-indol-2-yl]methyl acetate

https://huagongshe.com/reaction/2373489

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Xylyl bromideHCID 7721—
Reactant[5-(Benzyloxy)-1H-indol-2-yl]methyl acetateHCID 21964292—
Product[5-(Benzyloxy)-1-(4-methylbenzyl)-1H-indol-2-yl]methyl acetateHCID 21964286—

Reaction Steps

The title compound was prepared from [5-(benzyloxy)-1H-indol-2-yl]methyl acetate and 4-methylbenzyl bromide in substantially the same manner, as described in step 3 of Example 4. The product was obtained as a white solid. Mass-spectrum (ESI, [M+H)+) m/z 400. 1H NMR (300 MHz, DMSO-d6) δ 7.45 (d, 2H, J=8.34 Hz), 7.37 (t, 2H, J=7.19 Hz), 7.31 (d, 1H, J=7.30 Hz), 7.26 (d, 1H, J=7.56 Hz), 7.15 (d, 1H, J=2.44 Hz), 7.07 (d, 2H, J=8.76 Hz), 6.85 (d, 2H, J=8.81 Hz), 6.84 (s, 1H), 6.25 (s, 1H), 5.35 (s, 2H), 5.17 (s, 2H), 5.09 (s, 2H), 2.22 (s, 3H), 1.84 ppm (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459478B2
Source datasetuspto-grants-2008_12
ORD IDord-7cffba69b473439d8e3a05ea05762927
Source noteuspto-grants-2008_12