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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177070Generated: October 26, 2026

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

https://huagongshe.com/reaction/1177070

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 numberUS07842713B2
Source datasetuspto-grants-2010_11
ORD IDord-f18dbbf2800d41dcb6a3952f62647bed
Source noteuspto-grants-2010_11