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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 748673Erstellt: 25. Oktober 2026

Hexane → HCID 59750776, Verbindung

https://huagongshe.com/reaction/748673

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
Edukttert-Butyl(4-iodobutoxy)dimethylsilaneHCID 4250746—
Edukt2-(((4-Chlorophenyl)sulfonyl)methyl)-1,4-difluorobenzeneHCID 9901028—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
ProduktHCID 59750776HCID 59750776—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

In an argon gas stream and at −78° C., n-butyl lithium (a 1.57M hexane solution, 0.701 ml, 1.10 mmol) was added to a dimethoxyethane (5 ml) solution of the 2-[(4-chlorophenyl)sulfonylmethyl]-1,4-difluorobenzene (303 mg, 1.00 mmol) obtained in Example 5. The mixture was stirred at −78° C. for 1 hour and then, at room temperature for 30 minutes. The reaction mixture was cooled to −78° C., followed by the dropwise addition of 4-(t-butyldimethylsilyloxy)-1-iodobutane (0.260 ml, 1.00 mmol). While elevating the temperature of the reaction mixture to room temperature, stirring was conducted for 15 hours. Water was added to the reaction mixture, followed by extraction with diethyl ether. The extracts were combined, washed successively with water and brine, dried over MgSO4, and concentrated. The residue thus obtained was purified by medium-pressure chromatography on a silica gel column (8% ethyl acetate-hexane), whereby the title compound (401 mg, 82%) was obtained as a colorless solid. The resulting solid was recrystallized from hexane to yield colorless needle crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07399775B2
Quelldatensatzuspto-grants-2008_07
ORD IDord-bce6c0c610834911a1353b39d816ba56
Quellennotizuspto-grants-2008_07