ChemicalBook--->CAS DataBase List--->111721-75-6

111721-75-6

111721-75-6 Structure

111721-75-6 Structure
IdentificationMore
[Name]

2-Bromo-3-fluoroaniline
[CAS]

111721-75-6
[Synonyms]

2-BROMO-3-FLUOROANILINE
2-BROMO-3-FLUORO-PHENYLAMINE
[Molecular Formula]

C6H5BrFN
[MDL Number]

MFCD07369915
[Molecular Weight]

190.01
[MOL File]

111721-75-6.mol
Chemical PropertiesBack Directory
[Melting point ]

32-34 °C
[Boiling point ]

229.8±20.0 °C(Predicted)
[density ]

1.670
[Fp ]

94°(201°F)
[refractive index ]

1.5830
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

Crystalline
[pka]

1.52±0.10(Predicted)
[color ]

Off-white
[Water Solubility ]

Slightly soluble in water.
[InChI]

InChI=1S/C6H5BrFN/c7-6-4(8)2-1-3-5(6)9/h1-3H,9H2
[InChIKey]

XZRSXRUYZXBTGD-UHFFFAOYSA-N
[SMILES]

C1(N)=CC=CC(F)=C1Br
[CAS DataBase Reference]

111721-75-6(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

22-36-36/37/38-20/21/22
[Safety Statements ]

9-26-36/37-60
[RIDADR ]

2811
[WGK Germany ]

WGK 3
[Hazard Note ]

Harmful/Irritant
[HazardClass ]

6.1
[HS Code ]

29214200
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Irrit. 2
Hazard InformationBack Directory
[Chemical Properties]

Light yellow liquid
[Uses]

2-Bromo-3-fluoroaniline is used as pharmaceutical intermediate.
[Synthesis Reference(s)]

Journal of Heterocyclic Chemistry, 27, p. 2151, 1990 DOI: 10.1002/jhet.5570270755
[Synthesis]

2-Bromo-3-fluoronitrobenzene

59255-94-6

2-Bromo-3-fluoroaniline

111721-75-6

General procedure for the synthesis of 2-bromo-3-fluoroaniline from 2-bromo-3-fluoro nitrobenzene: 2-bromo-1-fluoro-3-nitrobenzene (1.0 g, 5.0 mmol) was dissolved in methanol (50 mL) at 0 °C, and NiCl? (2.2 g, 10 mmol) and NaBH? (0.50 g, 14 mmol) were added sequentially. After the addition was completed, the reaction mixture was stirred at 0 °C for 5 min. Subsequently, the reaction was quenched by the addition of water (20 mL) and extracted with ethyl acetate (20 mL x 3). The organic layers were combined, dried over anhydrous Na?SO? and concentrated under reduced pressure to afford 2-bromo-3-fluoroaniline (600 mg, 70% yield). The product was characterized by 1H NMR (400 MHz, CDCl?): δ 7.07-7.02 (m, 1H), 6.55-6.49 (m, 1H), 4.22 (br s, 2H).

[References]

[1] Patent: CN108002976, 2018, A. Location in patent: Paragraph 0045; 0047; 0050; 0051; 0060; 0069
[2] Journal of Organic Chemistry, 2011, vol. 76, # 9, p. 3416 - 3437
[3] Patent: US2007/244159, 2007, A1. Location in patent: Page/Page column 121
[4] Patent: US2011/98311, 2011, A1
[5] Patent: US2015/231142, 2015, A1. Location in patent: Paragraph 1674
Spectrum DetailBack Directory
[Spectrum Detail]

2-Bromo-3-fluoroaniline(111721-75-6)1HNMR
2-Bromo-3-fluoroaniline(111721-75-6)FT-IR
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