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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293469Generated: October 30, 2026

P-Anisidine → HCID 10476669, compound

https://huagongshe.com/reaction/1293469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantTriethylamineHCID 8471—
ReactantHCID 85966947HCID 85966947—
SolventChloroformHCID 6212—
ProductHCID 10476669HCID 1047666965%

Reaction Steps

Intermediate 63 (0.2 g, 0.62 mM) was dissolved in 40 ml of chloroform. To it was added p-anisidine (0.21 g, 1.66 mM), 0.19 g triethylamine and the reaction was refluxed for 18 hrs. Solvent was evaporated and the residue was extracted in ethyl acetate. The organic layer was washed with 10% HCl solution, brine and then dried over anhydrous Na2SO4. It was then evaporated to obtain the crude residue which was then purified over silica gel column using ethylacetate-hexane system to obtain the desired compound as beige solid with a yield of 65% (0.16 g); mp 190-192° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238725B2
Source datasetuspto-grants-2007_07
ORD IDord-9be862be32d44b87b62f562413e2d3c1
Source noteuspto-grants-2007_07