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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346879Generated: October 30, 2026

p-Anisoyl chloride → HCID 17956193, compound

https://huagongshe.com/reaction/346879

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantTin tetrachlorideHCID 24287—
ReactantHCID 17956195HCID 17956195—
SolventDichloromethaneHCID 6344—
ProductHCID 17956193HCID 17956193—

Reaction Steps

A solution of the product from Example 4(i) (1 g, 2.8 mmol) in dry DCM was stirred at 0° C. under nitrogen. Anisoyl chloride (4.9 mmol) was added followed by a solution of SnCl4 (1M DCM, 4.9 mmol). An immediate red colour occurred and stirring was continued for 2 hours. The reaction mixture was added carefully to 100 ml of ice-water and the aqueous was extracted with ethylacetate (3×100 Ml). The organic extracts were combined, dried (Na2SO4) and evaporated to give a bright yellow oil. This was purified by flash chromatography (silica flash) to give the title compound as a pale yellow solid. (0.8 g 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173061B2
Source datasetuspto-grants-2007_02
ORD IDord-976e7131d99e4023b98d49d0274e2994
Source noteuspto-grants-2007_02