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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607863Generated: October 30, 2026

Sodium hydride → HCID 22168537, compound

https://huagongshe.com/reaction/1607863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-Chloro-3-iodopropaneHCID 81363—
Reactant4-HydroxyphenylacetoneHCID 7019274—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
ProductHCID 22168537HCID 22168537—

Reaction Steps

A 4.50 g portion of p-hydroxyphenylacetone, prepared above, was dissolved in 80 mL of anhydrous dimethylformamide under a dry nitrogen atmosphere. With stirring 1.26 g of sodium hydride (as a 60% dispersion in oil) was added to the solution. After 3 minutes, 9.40 g of 1-chloro-3-iodopropane was quickly added. After stirring for approximately 18 hours, the reactionwas diluted with 300 mL hexane and 100 mL diethyl ether. The resulting mixture was washed with distilled water, 5% sodium hydroxide solution, andbrine. The remaining organic phase was dried and evaporated to dryness in vacuo. The yellow oil was purified by column chromatography over silica gel, using 22% ethyl acetate and 78% hexane. Appropriate fractions were pooled and solvents removed in vacuo to yield 3.06 g of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04868132
Source datasetuspto-grants-1989_09
ORD IDord-a8d3ef2fba224340a7dee101cc9ce233
Source noteuspto-grants-1989_09