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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947471Generated: November 3, 2026

Ethyl 6-(Benzyloxy)benzofuran-2-carboxylate → Ethyl 6-hydroxybenzofuran-2-carboxylate

https://huagongshe.com/reaction/1947471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 6-(Benzyloxy)benzofuran-2-carboxylateHCID 57810532—
CatalystPalladiumHCID 23938—
SolventEthanol ethylacetateHCID 21584252—
ProductEthyl 6-hydroxybenzofuran-2-carboxylateHCID 6678646970.1%

Reaction Steps

To a solution of 6-benzyloxy-benzofuran-2-carboxylic acid ethyl ester (8.1 g, 27 mmol) in EtOAc/EtOH (3/1, 130 mL) was added Pd/C (0.8 g). The reaction mixture was shaken in a Parr Shaker under H2 (50 psi, 12 h). The reaction mixture was filtered (Celite®), washed with EtOAC (400 mL) and EtOH (100 mL). The filtrate was concentrated and the resulting residue was purified by silica gel flash chromatography using EtOAc:hexanes (0-50%) to provide the title compound as colorless solid (3.9 g, 70%). MS (ESI): mass calcd. for C11H10O4, 206.1.0; m/z found, 207.1 [M+H]+. 1H NMR (400 MHz, CDCl3): 7.50 (d, J=8.6, 1H), 7.46 (d, J=0.8, 1H), 7.25-7.23 (m, 1H), 6.90 (dd, J=8.5, 2.2, 1H), 6.12 (s, 1H), 4.57-4.30 (m, 2H), 1.49-1.31 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399465B2
Source datasetuspto-grants-2013_03
ORD IDord-f1f3152353d7477fbf312eb715aad784
Source noteuspto-grants-2013_03