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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788949Generated: October 29, 2026

Pyridine → HCID 13770523, compound

https://huagongshe.com/reaction/1788949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChloroacetyl chlorideHCID 6577—
Reactant2H-Indol-2-one, 1-ethyl-1,3-dihydro-5-hydroxy-HCID 11805282—
SolventDichloromethaneHCID 6344—
ProductHCID 13770523HCID 13770523—

Reaction Steps

To a slurry of 100 g. (0.565 mole) of 1-ethyl-5-hydroxyoxindole in 91.3 ml. (1.13 moles) of pyridine and 565 ml. of dichloromethane at 0° C. was added dropwise a solution of 89.3 ml. (1.13 moles) of chloroacetyl chloride in 100 ml. of dichloromethane. The reaction mixture was allowed to stir for 15 minutes, and was then added to 1 l. of ice cold 2N hydrochloric acid and 500 ml. of dichloromethane. The aqueous layer was extracted once again with 300 ml. of dichloromethane and the combined organic extracts washed once with 500 ml. of a saturated brine solution, dried over magnesium sulfate and concentrated to give the desired product in quantitative yield. A small sample was crystallized from hexane, m.p. 53°-57° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04686224
Source datasetuspto-grants-1987_08
ORD IDord-e92da1eef89c454781325f5bee029024
Source noteuspto-grants-1987_08