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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373492Generated: October 31, 2026

1-(Bromomethyl)-4-(1,1-dimethylethyl)benzene → [5-(Benzyloxy)-1-(4-tert-butylbenzyl)-1H-indol-2-yl]methyl acetate

https://huagongshe.com/reaction/2373492

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Bromomethyl)-4-(1,1-dimethylethyl)benzeneHCID 87836—
Reactant[5-(Benzyloxy)-1H-indol-2-yl]methyl acetateHCID 21964292—
Product[5-(Benzyloxy)-1-(4-tert-butylbenzyl)-1H-indol-2-yl]methyl acetateHCID 21964282—

Reaction Steps

The title compound was prepared from [5-(benzyloxy)-1H-indol-2-yl]methyl acetate and 4-tert-butylbenzyl bromide in substantially the same manner, as described in step 3 of Example 4. The product was obtained as a white solid; mp: 132-133° C. Mass spectrum (ESI, [M+H]+) m/z 442. 1H NMR (400MHz, DMSO-d6) δ 7.45 (d, 2H, J=7.33 Hz), 7.38 (t, 2H, J=7.33 Hz), 7.32-7.27 (m, 4H), 7.16 (d, 1H, J=2.30 Hz), 6.88-6.84 (m, 3H), 6.53 (s, 1H), 5.36 (s, 2H), 5.18 (s, 2H), 5.08 (s, 2H), 1.77 (s, 3H), and 1.21 ppm (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459478B2
Source datasetuspto-grants-2008_12
ORD IDord-a0946dc3a3044fb993d018bde2927a0b
Source noteuspto-grants-2008_12