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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1637776Erstellt: 26. Oktober 2026

Crotyl chloride → HCID 54217396, Verbindung

https://huagongshe.com/reaction/1637776

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCrotyl chlorideHCID 11589—
EduktSodium hydrideHCID 24758—
EduktLithium iodideHCID 66321—
Edukt2-Chloro-3-hydroxy-4-iodo-6-(1-hydroxyethyl)-pyridineHCID 10709299—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 54217396HCID 5421739689%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

2-Chloro-3-hydroxy-6-(1-hydroxyethyl)-4-iodo-pyridine (4.49 g, 15 mmole) was dissolved in 25 ml dry dimethylformamide in an oven dried 50 ml two neck round bottom flask under nitrogen. The solution was cooled to 0° C., was treated with sodium hydride (600 mg, 15 mmole), and the mixture was stirred 1 h at room temperature. The mixture was treated with crotyl chloride (1.6 ml, 16.5 mmole) and one crystal of lithium iodide and the reaction mixture was stirred 20 h at room temperature. The reaction mixture was diluted with 100 ml ethyl acetate, was washed with 4×50 ml 50% saturated 1:1 sodium chloride/sodium bicarbonate, and was dried over anhydrous magnesium sulfate/potassium carbonate. The dried organics were concentrated in vacuo to a yellow oil which was crystallized from hexane to give 4.72 g (89%) of 3-(2-butenyloxy)-2-chloro-6-(1-hydroxyethyl)-4-iodo-pyridine as a white solid (Melting Point: 61-62.50° C.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06043248
Quelldatensatzuspto-grants-2000_03
ORD IDord-ffa29632cbe04195bf36b7f43db2f177
Quellennotizuspto-grants-2000_03