Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534768Generated: November 3, 2026

Heptanoic Acid → 2-Hexyl-5-(6-heptanoyloxynaphthalene-2-yl)-1,3,4-thiadiazole

https://huagongshe.com/reaction/1534768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHeptanoic AcidHCID 8094—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant4-PyrrolidinopyridineHCID 75567—
Reactant2-Hexyl-5-(6-hydroxynaphthalene-2-yl)-1,3,4-thiadiazoleHCID 136077200—
SolventDichloromethaneHCID 6344—
Product2-Hexyl-5-(6-heptanoyloxynaphthalene-2-yl)-1,3,4-thiadiazoleHCID 1990792881.5%

Reaction Steps

In a 30 ml-round-bottomed flask, 0.60 g (1.92 mM) of 2-hexyl-5-(6-hydroxynaphthalene-2-yl)-1,3,4-thiadiazole, 0.25 g (1.92 mM) of heptanoic acid were dissolved in 10 ml of dichloromethane. Under stirring, 0.39 g (1.89 mM) of N,N'-dicyclohexylcarbodiimide and 0.02 g of 4-pyrrolidinopyridine were successively added the above solution at room temperature, followed by stirring for 8 hours at room temperature. After the reaction, precipitated N,N'-dicyclohexylurea was filtered off and the filtrate was dried off under reduced pressure to obtain a solid. The solid was purified by silica gel column chromatography (eluent: toluene/ethyl acetate=3/1) and recrystallized from a mixture solvent (ethanol-ethyl acetate) to obtain 0.42 g of 2-hexyl-5-(6-heptanoyloxynaphthalene-2-yl)-1,3,4-thiadiazole (Yield: 81.5 %). ##STR139##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05091109
Source datasetuspto-grants-1992_02
ORD IDord-33406f5327e9400d860c979c99a09d01
Source noteuspto-grants-1992_02