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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081561Generated: October 30, 2026

Potassium Iodide → Methyl 4-(acetylamino)-2-(1,1-dimethyl-2-propynyloxy)benzoate

https://huagongshe.com/reaction/2081561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
Reactant1-Butyne, 3-chloro-3-methyl-HCID 70679—
ReactantMethyl 4-acetamidosalicylateHCID 77719—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-(acetylamino)-2-(1,1-dimethyl-2-propynyloxy)benzoateHCID 1978327310.1%

Reaction Steps

To a solution of 310 parts of methyl 4-(acetylamino]-2-hydroxybenzoate in 2820 parts of N,N-dimethylformamide there were added portionwise 71 parts of a dispersion of sodium hydride in mineral oil (50%) and, after stirring for 1 hour at room temperature, one crystal of potassium iodide and 172 parts of 3-chloro-3-methyl-1-butyne under a nitrogen atmosphere. The whole was stirred for 24 hours at 90° C. and was then poured into NaOH 10% (aq.). The product was extracted with dichloromethane and the extract was dried, filtered and evaporated. The residue was successively stirred in petroleumether and dissolved in dichloromethane. The latter solution was washed with water, NaOH 10% and water and was then dried, filtered and evaporated. The residue was purified by column chromatography (silica gel; CH2Cl2). The eluent of the desired fraction was evaporated, yielding in two fractions 41 parts (10.1%) of methyl 4-(acetylamino)-2-(1,1-dimethyl-2-propynyloxy)benzoate (interm. 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05185335
Source datasetuspto-grants-1993_02
ORD IDord-91c7e1f71e6c4f4ab013ffbd53f1cf37
Source noteuspto-grants-1993_02