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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700417Generated: October 26, 2026

Water → 3-[3'(3",4",5"-Trimethoxyphenyl)propionyl]-2-(4'methoxyphenyl)-6-methoxybenzo[b]thiophene

https://huagongshe.com/reaction/1700417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant6-Methoxy-2-(4-methoxyphenyl)benzo[b]thiopheneHCID 850941—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant3-(3',4',5'-Trimethoxyphenyl)propionyl chlorideHCID 14650097—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product3-[3'(3",4",5"-Trimethoxyphenyl)propionyl]-2-(4'methoxyphenyl)-6-methoxybenzo[b]thiopheneHCID 10074396—

Reaction Steps

To a well-stirred solution of 2-(4′-methoxyphenyl)-6-methoxybenzo[b]thiophene (0.206 g, 0.762 mmol) and 3-(3′,4′,5′-trimethoxyphenyl)propionyl chloride (0.390 g, 1.51 mmol) in CH2Cl2 (50 mL) was added AlCl3 (0.520 g, 3.89 mmol) portion-wise over a 15 minute period. After 18 hours (total reaction time), water was added, and the product was isolated initially by extraction with CH2Cl2 and subsequently by extraction with EtOAc. The organic layers were separately washed sequentially with NaHCO3 (sat) and brine and then combined and dried over MgSO4. Purification by flash chromatography (silica gel, 70:30 EtOAc/hexane) afforded the title compound as an off-white solid. 1H-NMR (CDCl3, 360 Mhz): δ=7.92 (d, J=8.9 Hz, 1H, ArH), 7.35 (d, J=8.7 Hz, 2H, ArH), 7.25 (m, 1H, ArH), 7.04 (dd, J=8.9, 2.4 Hz, 1H, ArH), 6.93 (d, J=8.7 Hz, 2H, ArH), 6.15 (s, 2H, ArH) 3.88 (s, 3H, —OCH3), 3.85 (s, 3H, —OCH3), 3.78 (s, 3H, —OCH3), 3.72 (s, 6H, —OCH3), 3.80 (t, 2H, CH2), 3.70 (t, 2H, CH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350777B2
Source datasetuspto-grants-2002_02
ORD IDord-cf8f4ddc16a14b1cb3a0730300af4791
Source noteuspto-grants-2002_02