ChemicalBook--->CAS DataBase List--->898832-40-1

898832-40-1

898832-40-1 Structure

898832-40-1 Structure
IdentificationBack Directory
[Name]

8-FLUORO-3,4-DIHYDRO-2H-BENZO[1,4]OXAZINE HYDROCHLORIDE
[CAS]

898832-40-1
[Synonyms]

8-Fluoro-3,4-dihydro-2H-benzo[1,4]oxazine
2H-1,4-Benzoxazine, 8-fluoro-3,4-dihydro-
8-Fluoro-3,4-dihydro-2H-benzo[b][1,4]oxazine
8-Fluoro-3,4-dihydro-2H-benzo[1,4]oxazine 1HCl salt
8-FLUORO-3,4-DIHYDRO-2H-BENZO[1,4]OXAZINE HYDROCHLORIDE
[Molecular Formula]

C8H8FNO
[MDL Number]

MFCD08544330
[MOL File]

898832-40-1.mol
[Molecular Weight]

153.15
Chemical PropertiesBack Directory
[Boiling point ]

238℃
[density ]

1.200
[Fp ]

98℃
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

Brown to reddish brown Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HS Code ]

2934999090
Spectrum DetailBack Directory
[Spectrum Detail]

8-FLUORO-3,4-DIHYDRO-2H-BENZO[1,4]OXAZINE HYDROCHLORIDE(898832-40-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

8-FLUORO-2H-BENZO[B][1,4]OXAZIN-3(4H)-ONE

560082-51-1

8-FLUORO-3,4-DIHYDRO-2H-BENZO[1,4]OXAZINE HYDROCHLORIDE

898832-40-1

8-Fluoro-2H-1,4-benzoxazin-3(4H)-one (1.0 g, 5.9 mmol) was used as starting material, which was dissolved in THF (25 mL) and stirred to form a suspension at 0 °C to -5 °C. Subsequently, a THF solution of lithium aluminum hydride (7 mL, 1 M) was slowly added dropwise. After the dropwise addition, the reaction mixture was warmed to room temperature and stirring was continued for 2 hours. Upon completion of the reaction, the mixture was carefully poured into ice water to quench the reaction and extracted with ethyl acetate. The organic phases were combined, dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to remove the solvent. The resulting residue was ground with ether to afford 8-fluoro-3,4-dihydro-2H-benzo[1,4]oxazine (0.8 g, 87% yield) as a dark brown solid. Mass spectrum (ESI+): m/z 154 [M+H]+. 1H NMR (DMSO-d6): δ 3.27 (2H, m), 4.11 (2H, m), 6.05 (1H, br s), 6.34 (2H, m), 6.58 (1H, m).

[References]

[1] Patent: WO2011/144578, 2011, A1. Location in patent: Page/Page column 30
[2] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 16, p. 4700 - 4704
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