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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 59686Erstellt: 24. Oktober 2026

Hydrochloric Acid → 5-(3-Bromopropyl)thiophene-2-carboxylic acid

https://huagongshe.com/de/reaction/59686

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium ChlorideHCID 5234—
Edukt2-Thiophenecarboxylic acidHCID 10700—
Edukt2,2-DibromopropaneHCID 11658—
EduktAmmonium ChlorideHCID 25517—
EduktLithium diisopropylamideHCID 2724682—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-(3-Bromopropyl)thiophene-2-carboxylic acidHCID 53984314123,5%

Reaktionsschritte

To a solution consisting of thienoic acid (10 g, 78 mmol) in THF (150 mL) at −78° C. was added an LDA solution (85 mL, 170 mmol, 2 M in heptanes/THF/ethylbenzene, Sigma-Aldrich) dropwise over 20 minutes, and the reaction mixture was stirred 40 minutes. To the reaction mixture was then added dibromopropane (23.8 g, 117 mmol) in one portion, and the reaction mixture was allowed to warm to room temperature and was stirred for 3 days. To the reaction mixture was added 50 mL each of a saturated aqueous solution of ammonium chloride, a saturated aqueous solution of sodium chloride, and 6 N HCl. The organic material was extracted with ethyl acetate and the organic layer was dried over sodium sulfate, filtered, and concentrated to afford the title compound as a yellow oil (24.0 g). The product was used without further purification; TLC Rf 0.5 (solvent system: 30:70:1 v/v ethyl acetate-hexanes-acetic acid).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440919B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-6d56a827b0c04ac2a2287ec46d1153ea
Quellennotizuspto-grants-2016_09