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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 477500Erstellt: 24. Oktober 2026

Cyclopropanecarbonyl chloride → HCID 14819887, Verbindung

https://huagongshe.com/de/reaction/477500

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclopropanecarbonyl chlorideHCID 77637—
Edukt5-MethylisoxazoleHCID 79833—
EduktLithium diisopropylamideHCID 2724682—
EduktLithiumHCID 3028194—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
ProduktHCID 14819887HCID 1481988729,9%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

n-Buyllithium (19.44 ml, 52.5 mmole of a 2.7 M solution in hexane) was added at -15° C. to a solution of diisopropylalmine (5.31g, 52.5 mmole) in 80 ml of dry THF. After 10 min the cooling bath was lowered to -70° C. and 5-methylisoxazole (4.15 g, 50 mmoles) was added to the lithium diidopropylalmine (LDA) solution followed in 30 min by the dropwise addition of cyclopropanecarboxylic acid chloride (5.33 g, 50 mmoles) in 15 ml of THF. The reaction mixture was then stirred at -78° C. for 30 min and at ambient temperature for 2 h. The solvents were evaporated and the residue was partitioned between ether, 30 ml of water and 13 ml of 4 N NaOH. The aqueous layer was separated, acidified with 6 N HCl and extracted with two portions of ether. The extracts were dried and evaporated to a slushy solid that was cchromatographed on 100 g of silica gel using methylene chloride-Skellysolve B (95:5). The appropriate fractions were combined and concentrated to yield 2.26 g of the title compound as a yellow-tinted solid, mp 62°-63.5° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04888357
Quelldatensatzuspto-grants-1989_12
ORD IDord-09ac9aefe91141aa93355a3918e89440
Quellennotizuspto-grants-1989_12