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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 57778Erstellt: 23. Oktober 2026

Dichloromethane → (3-Phenyl-5-isoxazolyl)methanol

https://huagongshe.com/de/reaction/57778

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktPropargyl alcoholHCID 7859—
Edukt(Z)-Benzaldehyde oximeHCID 12143—
EduktChlorosuccinimideHCID 31398—
LösungsmittelTriethylamineHCID 8471—
Produkt(3-Phenyl-5-isoxazolyl)methanolHCID 276341776,8%

Reaktionsschritte

10.0 mmol of Benzaldehyde oxime and 30 ml of dry dichloromethane were added into a 250 ml single-necked round-bottom flask. After the addition of 1.60 g (12.0 mmol) of N-chlorosuccinimide (NCS) under stirring, the mixture was slightly heated until NCS was completely dissolved. 0.56 g (10.0 mmol) of 2-propyn-1-ol was added dropwise, and then 20 ml solution of triethylamine in dichloromethane containing 10.1 g (10.0 mmol) of triethylamine was slowly added dropwise. After the addition was complete, the system was refluxed. After the completion of the reaction monitored by TLC, the mother liquor was washed with water, dried over anhydrous sodium sulfate and was separated on column (Vpetroleum ether:Vethyl acetate=5:1-2:1) to give 3-phenyl-5-hydroxymethyl-isoxazole in 76.8% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434741B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-3d742c6dc93b4aa08164691e7afb0562
Quellennotizuspto-grants-2016_09