Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424103Generated: October 25, 2026

Tetrahydrofuran → 5-Isopropenyl-2,4-dimethoxy-benzoic acid methyl ester

https://huagongshe.com/reaction/424103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantCesium carbonateHCID 10796—
ReactantMethyl 5-bromo-2,4-dimethoxybenzoateHCID 3859236—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product5-Isopropenyl-2,4-dimethoxy-benzoic acid methyl esterHCID 59263148—

Reaction Steps

To potassium isopropylidene trifluoroborate (4.87 g, 32.7 mmol) and 5-bromo-2,4-dimethoxybenzoic acid methyl ester (7.5 g, 27.3 mmol) in THF (195 ml) was added Cs2CO3 (26.6 g, 81.8 mmol) in water (39 ml). The reaction was degassed and Pd(PPh3)4 (1.58 g, 1.36 mmol) added. The reaction was heated at reflux for three days then quenched by adding water and extracted with EtOAc (×2). The combined organic layers were washed with brine, dried (MgSO4), filtered and evaporated to leave an orange solid. The product was taken up in EtOAc again and the precipitate filtered. The filtrate was evaporated to dryness to yield 5-isopropenyl-2,4-dimethoxy-benzoic acid methyl ester (6.2 g). 1H NMR (Me-d3-OD) 7.68 (1H, s), 6.66 (1H, s), 5.10-5.08 (1H, m), 5.02-5.00 (1H, m), 3.93 (3H, s), 3.92 (3H, s), 3.84 (3H, s), 2.08-2.06 (3H, m). MS: [M+H]+ 237.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101648B2
Source datasetuspto-grants-2012_01
ORD IDord-08a9916e00dd4ab2bdb830d9bb8bc2c7
Source noteuspto-grants-2012_01