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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700420Generated: November 1, 2026

Water → Benzo(B)Thiophene

https://huagongshe.com/reaction/1700420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzoyl chloride, 3,4,5-trimethoxy-HCID 78282—
Reactant2-(4-Methoxyphenyl)benzothiopheneHCID 4137391—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductBenzo(B)ThiopheneHCID 722181.5%

Reaction Steps

To a well-stirred solution of 2-(4′-methoxyphenyl)benzo[b]thiophene (0.081 g, 0.32 mmol) and 3,4,5-trimethoxybenzoyl chloride (0.148 g, 0.64 mmol) in CH2Cl2 (15 mL) was added AlCl3 (0.144 g, 1.08 mmol) portion-wise over a 5 minute period. After 3 h 20 min, 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, 90:10 hexane/EtOAc then with 80:20 hexane/EtOAc) afforded desired benzo[b]thiophene (0.035 g, 26%) as white solid. 1H-NMR-(CDCl3, 360 MHz) δ7.87 (m, 1H, ArH), 7.78 (m, 1H, ArH), 7.37 (m, 4H, ArH), 7.07 (s, 2H, ArH), 6.76 (d, J=6.7, 2H, ArH), 3.84 (s, 3H, —OCH3), 3.75 (s, 3H, —OCH3), 3.73 (S, 6H, —OCH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350777B2
Source datasetuspto-grants-2002_02
ORD IDord-04fb1fc13b0e47c3bc64bf6d7d37ae12
Source noteuspto-grants-2002_02