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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710382Generated: October 29, 2026

3-Hydroxybenzaldehyde → 3-Benzyloxybenzaldehyde

https://huagongshe.com/reaction/710382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
SolventDimethylformamideHCID 6228—
Product3-BenzyloxybenzaldehydeHCID 7434276.4%

Reaction Steps

A mixture of benzyl bromide (1.4 g; 8.2 mmol), 3-hydroxybenzaldehyde (1.0 g; 8.2 mmol) and Cs2CO3 (2.67 g; 8.2 mmol) in anhydrous DMF (5 ml) was stirred overnight at room temperature under N2. After evaporation of solvent in vacuo, the residue was diluted to 20 ml with CH2Cl2, washed with H2O, brine, dried over anhydrous MgSO4, filtered and filtrate evaporated to dryness to give the title compound (1.33 g; 76%) as creamy foam. 1H-NMR (CDCl3) 5.11 (s, 2H); 7.2-7.48 (m, 9H); 9.96 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181182B2
Source datasetuspto-grants-2015_11
ORD IDord-b0fc5e05417e43f7a6d17d1df81df3c2
Source noteuspto-grants-2015_11