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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196799Generated: October 31, 2026

Hydrochloric Acid → 4-(5-Dodecyl-2-pyrimidinyl)phenyl 5-hexylthiophene-2-carboxylate

https://huagongshe.com/reaction/1196799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
Reactant5-Hexylthiophene-2-carboxylic acid chlorideHCID 13128272—
Reactant4-(5-Dodecyl-2-pyrimidinyl)phenolHCID 136035706—
SolventWaterHCID 962—
Product4-(5-Dodecyl-2-pyrimidinyl)phenyl 5-hexylthiophene-2-carboxylateHCID 1989629130.2%

Reaction Steps

15 ml of pyridine was added to 0.80 g (2.36×10-3 mol) of 4-(5-dodecyl-2-pyrimidinyl)phenol, followed by cooling on an iced water bath. To the mixture, 0.54 g (2.36×10-3 mol) of 5-hexylthiophene-2-carboxylic chloride was added, followed by stirring for 5 hours at room temperature. After the reaction, the reaction mixture was poured into 100 ml of water and acidified with conc. hydrochloric acid, followed by three times of extraction with 50 ml of isopropyl ether. The organic layer was washed with water repeatedly until the washing liquid reacted neutrality, followed by drying with anhydrous magnesium sulfate and distilling-off of the solvent to obtain a crude product. The crude product was purified by silica gel column chromatography with the use of a hexane/ethyl acetate =10/1 mixture solvent and recrystallized from ethanol to obtain 0.38 g of a pure product (yield: 30.2%). ##STR29##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116530
Source datasetuspto-grants-1992_05
ORD IDord-444b0639d3854c2586e0b767a1177cae
Source noteuspto-grants-1992_05