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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868258Generated: October 29, 2026

p-Anisoyl chloride → HCID 14257798, compound

https://huagongshe.com/reaction/868258

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 14257796HCID 14257796—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 14257798HCID 14257798189.3%

Reaction Steps

To p-anisoyl chloride (205 g) in 1,2-dichloroethane (2 L), cooled to 0° C., was added AlCl3 (240 g). The reaction mixture was warmed to room temperature and a solution of 7-hydroxy-3,5,6-trimethylbenzofuran (51 g) in 1,2-dichloroethane (400 mL) was added dropwise. The reaction was stirred for 51/2 h then quenched with H2O (2 L). The organic layer was separated and the aqueous layer was extracted with CH2Cl2. The combined extracts were washed with 25% NH4OAc buffer, dried (Na2SO4) and filtered on silica gel to give 170 g of crude material which was used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04778805
Source datasetuspto-grants-1988_10
ORD IDord-5ae1b1322de04653ad4095a97d23d956
Source noteuspto-grants-1988_10