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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206731Generated: November 1, 2026

Phenetole → HCID 71110860, compound

https://huagongshe.com/reaction/2206731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenetoleHCID 7674—
ReactantOxalyl chlorideHCID 65578—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 71076950HCID 71076950—
ReactantHCID 86714064HCID 86714064—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 71110860HCID 7111086079.8%

Reaction Steps

After dissolving crude 7-bromo-4-chlorobenzo[b]thiophene-5-carboxylic acid 97 (847 mg, 2.91 mmol) in CH2Cl2, (COCl)2 (0.49 mL, 5.82 mmol) and catalytic amount DMF was added carefully at 0° C. The resulting solution was stirred overnight at room temperature. The volatiles were evaporated under reduced pressure and dried in vacuo. The crude compound was used for the next step without further purification. To a solution of crude 7-bromo-4-chlorobenzo[b]thiophene-5-carbonyl chloride in CH2Cl2 (50 mL) was added ethoxybenzene (462 mg, 3.78 mmol) and AlCl3 (464 mg, 3.49 mmol) at 0° C. After warming the reaction mixture up to room temperature, it was stirred for 4 hours. The resulting compound was quenched with aq. NH4Cl solution and the normal work-up with EtOAc was conducted. Purification by silica gel chromatography gave the title compound (917 mg, 79.8%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371303B2
Source datasetuspto-grants-2016_06
ORD IDord-6ecf68f8ac914e419720ae902d1e1c01
Source noteuspto-grants-2016_06