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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Heptanoic Acid | HCID 8094 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 4-Pyrrolidinopyridine | HCID 75567 | — |
| Reactant | 2-Hexyl-5-(6-hydroxynaphthalene-2-yl)-1,3,4-thiadiazole | HCID 136077200 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Hexyl-5-(6-heptanoyloxynaphthalene-2-yl)-1,3,4-thiadiazole | HCID 19907928 | 81.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05091109 |
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| Source dataset | uspto-grants-1992_02 |
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| ORD ID | ord-33406f5327e9400d860c979c99a09d01 |
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| Source note | uspto-grants-1992_02 |
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