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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419128Generated: November 3, 2026

Water → HCID 15411219, compound

https://huagongshe.com/reaction/1419128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3,5-Dimethoxybenzoyl chlorideHCID 87003—
Reactant6-Methoxy-2-(4-methoxyphenyl)benzo[b]thiopheneHCID 850941—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 15411219HCID 1541121948%

Reaction Steps

To a well-stirred solution of 2-(4--methoxyphenyl)-6-methoxybenzo[b]thiophene (0.615 g, 2.27 mmol) and 3,5-dimethoxybenzoyl chloride (1.37 g, 6.83 mmol) in CH2Cl2 (45 mL) was added AlCl3 (1.21 g, 9.09 mmol) portion-wise over a 15 minute period. After 17 hours, 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 with brine and then combined and dried over MgSO4. Purification by flash chromatography (silica gel, 60:40 EtOAc/hexane) afforded the title compound (0.475 g, 1.09 mmol, 48%) as an off-white solid. Recrystallization (hexane/ethanol) afforded a highly pure, crystalline sample with mp 114°-120° C.: 1H-NMR (CDCl3, 360 Mhz): δ=7.59 (d,J=8.9 Hz, 1H, ArH), 7.32 (d,J=8.5 Hz, 2H, ArH), 7.32 (d,J=2.4 Hz, 1H, ArH), 6.98 (dd,J=9.0,2.4 Hz, 1H, ArH), 6.94 (d,J=2.1 Hz, 2H, ArH), 6.76 (d,J=8.7 Hz, 2H, ArH), 6.52 (t,J=2.4 Hz, 1H, ArH), 3.89 (s,3H, --OCH3), 3.76 (s,3H, --OCH3), 3.71 (s,6H, --OCH3); 13C-NMR (CDCl3, 90 Mhz): δ=194.0, 160.5, 159.8, 157.7, 143.9, 140.0, 139.3, 133.8, 130.3, 130.1, 126.0, 124.1, 114.9, 114.0, 107.6, 106.1, 104.4, 55.6, 55.5, 55.2. HRMS (EI) M+ calcd for C25H22O5S 434.1188, found 434.1245.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05886025
Source datasetuspto-grants-1999_03
ORD IDord-c50f353cca3444ebbb561be7a4186c76
Source noteuspto-grants-1999_03