Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424364Generated: October 30, 2026

Chlorobenzene → HCID 86700907, compound

https://huagongshe.com/reaction/1424364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorobenzeneHCID 7964—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant1-(6-Chloro-4-methoxy-2-benzofuranyl)ethanoneHCID 86700906—
ProductHCID 86700907HCID 8670090788%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 1-(6-chloro-4-methoxybenzofuran-2-yl)ethanone (Example 37C, 1.43 g, 6.37 mmol) in chlorobenzene (15 mL, 148 mmol) was added aluminum chloride (3.40 g, 25.5 mmol) in portions over a period of 10 minutes. The reaction vessel was then sealed and heated at 100° C. for 40 minutes, then cool to r.t. and poured onto crushed ice (rinsed stirring bar with EtOAc). This was stirred for 30 minutes, then extracted with ethyl acetate. The organic phase was dried (MgSO4), filtered and concentrated to dryness. The residue was purified by ISCO using hexanes/EtOAc as eluent. Fractions containing the desired product were concentrated to give the title material (1.18 g, 5.60 mmol, 88% yield) as a light brown solid. LC (Method A): 1.783 min. LCMS (APCI) calcd for C10H8ClO3 [M+H]+ m/z 211.02. found 211.0. 1H NMR (CDCl3, 400 MHz) δ ppm: 11.01 (s, 1H), 7.89 (s, 1H), 6.72 (s, 1H), 2.52 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927688B2
Source datasetuspto-grants-2015_01
ORD IDord-da0f4cf96dea4c839f5e800d70a23201
Source noteuspto-grants-2015_01