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HRID 1600996Erstellt: 27. Oktober 2026

Methyl iodide → 4-(tert-Butoxy)-2,3,6-trifluoro-5-methylpyridine

https://huagongshe.com/reaction/1600996

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
Edukt4-t-Butoxy-2,3,6-trifluoropyridineHCID 10608547—
EduktLithium diethylamideHCID 11137085—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(tert-Butoxy)-2,3,6-trifluoro-5-methylpyridineHCID 10751339—

Reaktionsschritte

A freshly prepared solution of lithium diethylamide (LDA) (58.21 mmol) in 30 mL of THF at -78° C. was added to 10.0 g (48.74 mmol) of 4-t-butoxy-2,3,6-trifluoropyridine in 50 mL of THF at -78° C, and the reaction was stirred for 50 min. To the reaction mixture was added 4.3 mL (69.07 mmol) of methyl iodide, and the mixture was stirred at -78° C. for 1 hour and stirred at ambient temperature for 16 hours. The reaction was quenched with saturated NH4Cl solution, extracted with hexane, and the extracts washed with water, dried over MgSO4 and concentrated to give 4-t-butoxy-2,3,6-trifluoro-5-methylpyridine as a pale yellow oil, which was taken directly to the next step. MS (220) (M+H)+ ; 1H NMR (CDCl3)∂: 1.47 (m, 9H), 2.12 (m, 3H). 19F NMR (CDCl3, CFCl3 as reference)∂: 75.91 (dd apparent, J1 =15.0, J2 =22.1 Hz), 93.17 (dd apparent, J1 =15.0, J2 =22.1 Hz), 156.54 (m).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05977133
Quelldatensatzuspto-grants-1999_11
ORD IDord-81a27554c02e4f1b887385db98acc972
Quellennotizuspto-grants-1999_11