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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607609Generated: October 31, 2026

Pyridine → 3-Chloroacetyl-5-(benzyloxy)indole

https://huagongshe.com/reaction/1607609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChloroacetyl chlorideHCID 6577—
Reactant5-BenzyloxyindoleHCID 14624—
ReactantDiethylether waterHCID 21584184—
Solvent1,4-DioxaneHCID 31275—
Product3-Chloroacetyl-5-(benzyloxy)indoleHCID 10891912—

Reaction Steps

5-(Benzyloxy)indole in dioxane containing pyridine was stirred for 1 hr. at 65° C. under nitrogen while chloroacetyl chloride in dioxane was added dropwise. The reaction mixture was stirred for another 1 hr., then poured into diethyl ether-water. The precipitate was collected by filtration and washed thoroughly with cold Et2O to yield 19, an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04866084
Source datasetuspto-grants-1989_09
ORD IDord-80b58256898549e4b404b9fe585b36dc
Source noteuspto-grants-1989_09