Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38640Generated: October 26, 2026

Ethanol → 2-Benzyloxybenzoic acid

https://huagongshe.com/reaction/38640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-(benzyloxy)benzoateHCID 345928—
SolventWaterHCID 962—
Product2-Benzyloxybenzoic acidHCID 181058184.6%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a suspension of 73 (4.0 g, 15.6 mmol) in H2O (150 ml) were added NaOH (3.1 g, 78.0 mmol) and EtOH (5 ml). The mixture was reflux for 12 h, and cooled to 25° C. The solid was filtered out and the filtrate was acidified with 2N HCl. The precipitate was collected and washed with H2O. The crude product was recrystallized from to give 78 as white solid. (3.0 g, 13.2 mmol). Yield: 84.6%; mp 73-75° C.; MS (EI, 70 eV): m/z 228.3 (M+); 1H-NMR (CDCl3, 200 MHz): δ 5.27 (s, 2H), 7.08-7.54 (m, 8H), 6.93 (dd, J=8.0, 1.8 Hz, 1H); 13C-NMR (CDCl3, 50 MHz) δ: 165.43, 157.40, 135.02, 134.34, 133.88, 129.16, 127.92, 122.44, 118.09, 113.11, 72.23; Anal. Calcd for C14H12O3: C, 73.67; H, 5.30.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524740B2
Source datasetuspto-grants-2013_09
ORD IDord-11b9b0ab40304925a3d101c2731ff662
Source noteuspto-grants-2013_09