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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649939Generated: October 29, 2026

Potassium Iodide → Methyl 5-benzoylamino-5,6,7,8-tetrahydro-naphth-1-yl-oxyacetate

https://huagongshe.com/reaction/1649939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantMethyl chloroacetateHCID 7295—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Benzoylamino-1-hydroxy-5,6,7,8-tetrahydro-naphthaleneHCID 14014955—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-benzoylamino-5,6,7,8-tetrahydro-naphth-1-yl-oxyacetateHCID 14014967—

Reaction Conditions

Temperature50 °C

Reaction Steps

50 mmol of 5-benzoylamino-1-hydroxy-5,6,7,8-tetrahydro-naphthalene and 100 ml of anhydrous potassium potassium carbonate are stirred at 50° C. in 100 ml of absolute dimethylformamide for 20 minutes. A solution of 60 mmol of methyl chloroacetate and 25 mmol of potassium iodide in 25 ml dimethylformamide is added dropwise and the mixture is stirred at 50° C. for 6 to 8 hours. It is filtered under the influence of heat, the residue is rinsed thoroughly with ethyl acetate and the filtrate is evaporated. The residue is stirred in a mixture of 10% strength NaOH and ethyl acetate or tetrahydrofuran for 10 minutes. The ethyl acetate phase is extracted by shaking once with 10% strength NaOH, dried over Na2SO4 and evaporated. The residue is recrystallized from ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04921998
Source datasetuspto-grants-1990_05
ORD IDord-f84af81b285a41fa8277dda8c220d603
Source noteuspto-grants-1990_05