Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643543Generated: October 25, 2026

Lithium Chloride → 5-Methoxy-2-methyl-benzofuran-7-carboxylic acid methyl ester

https://huagongshe.com/reaction/1643543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium ChlorideHCID 433294—
Reactant3-Allyl-2-hydroxy-5-methoxy-benzoic acid methyl esterHCID 14838669—
CatalystCupric acetateHCID 8895—
CatalystPalladium ChlorideHCID 24290—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-Methoxy-2-methyl-benzofuran-7-carboxylic acid methyl esterHCID 59560465100.9%

Reaction Steps

To a solution of 3-allyl-2-hydroxy-5-methoxy-benzoic acid methyl ester (4b) (1.48 g, 6.66 mmol) in DMF (30 mL) was added Cu(OAc)2 (3.63 g, 19.98 mmol), LiCl (847 mg, 19.98 mmol) in H2O (1 mL) and PdCl2 (24 mg, 0.133 mmol). The reaction mixture was stirred at RT for 3 h, quenched with H2O (100 mL) and NH4OH (5 mL) and extracted with EtOAc (100 mL). The organic layer was washed with H2O (100 mL), dried over MgSO4 and concentrated. The residue was purified by flash column chromatograph eluting with 10-15% EtOAc/hexane to give colorless oil (1.48 g, 48%). 1H NMR (400 MHz, CDCl3) δ 7.43 (d, J=2.53 Hz, 1 H) 7.17 (d, J=2.53 Hz, 1 H) 6.36 (s, 1 H) 4.00 (s, 3 H) 3.87 (s, 3 H) 2.51 (s, 3 H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119624B2
Source datasetuspto-grants-2012_02
ORD IDord-acc340d7a3a844cf94629aad272434ef
Source noteuspto-grants-2012_02