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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875593Generated: October 25, 2026

3-Hydroxybenzaldehyde → 3-(5-Benzyloxypentoxy)-benzaldehyde

https://huagongshe.com/reaction/875593

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
Reactant5-(benzyloxy)pentyl MethanesulfonateHCID 44627117—
Product3-(5-Benzyloxypentoxy)-benzaldehydeHCID 86637621—

Reaction Steps

Alkylation reaction of 3-hydroxybenzaldehyde with 5-(benzyloxy)pentyl methanesulfonate gave 3-(5-(benzyloxy)pentyloxy)benzaldehyde as a clear oil. Yield (1.3 g, 66%): 1H NMR (400 MHz, CDCl3) δ 9.97 (s, 1H), 7.42-7.46 (m, 2H), 7.25-7.39 (m, 6H), 7.15-7.18 (m, 1H), 4.51 (s, 2H), 4.02 (t, J=6.4 Hz, 2H), 3.51 (t, J=6.4 Hz, 2H), 1.82-1.89 (m, 2H), 1.68-1.76 (m, 2H), 1.54-1.62 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981153B2
Source datasetuspto-grants-2015_03
ORD IDord-fee5a8328e6342d8bebe3c199104de22
Source noteuspto-grants-2015_03