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HRID 277867Erstellt: 26. Oktober 2026

2,2,2-Trifluoro-1-methoxyethanol → 6-bromo-4,4-dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazine

https://huagongshe.com/reaction/277867

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,2,2-Trifluoro-1-methoxyethanolHCID 9892—
EduktSulfuric acid magnesium salt (1:1)HCID 24083—
Edukt2-(2-Amino-5-bromophenyl)propan-2-olHCID 12042275—
LösungsmittelTolueneHCID 1140—
Produkt6-bromo-4,4-dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazineHCID 23435572—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 2-(2-amino-5-bromo-phenyl)-propan-2-ol (5 g, 21.7 mmol), trifluoroacetaldehyde methyl hemiacetal (5 mL), and magnesium sulfate (10 g) in toluene (75 mL) was heated at 80° C. under nitrogen. After disappearance of the starting material, the reaction was filtered through a pad of silica gel and the filtrate dried over sodium sulfate and concentrated to give 6-bromo-4,4-dimethyl-2-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazine as an amorphous solid: 1H-NMR (DMSO-d6) δ 7.31 (d, 1H, J=1.99 Hz), 7.19 (dd, 1H, J=8.73, 2.38 Hz), 6.88 (s, 1H), 6.74 (d, 1H, J=8.33 Hz), 5.32 (m, 1H), 1.52 (s, 6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06358948B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-a1ac86a113da49aa8e9fce5c94023f0f
Quellennotizuspto-grants-2002_03