ChemicalBook--->CAS DataBase List--->2107-43-9

2107-43-9

2107-43-9 Structure

2107-43-9 Structure
IdentificationBack Directory
[Name]

N,N-DIMETHYL-3-FLUOROANILINE
[CAS]

2107-43-9
[Synonyms]

3-Fluoro-N,N-diMethylaniline
N,N-DIMETHYL-3-FLUOROANILINE
1-Fluoro-3-(dimethylamino)benzene
3-Fluoro-N,N-dimethyl-benzenamine
1-(DIMETHYLAMINO)-3-FLUOROBENZENE
Benzenamine, 3-fluoro-2,4-dimethyl-
Benzenamine, 3-fluoro-N,N-dimethyl-
[Molecular Formula]

C8H10FN
[MDL Number]

MFCD01862042
[MOL File]

2107-43-9.mol
[Molecular Weight]

139.17
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

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

26-36/37/39
[RIDADR ]

1993
[Hazard Note ]

Irritant
[HazardClass ]

3
[PackingGroup ]

[HS Code ]

2921490090
Hazard InformationBack Directory
[Synthesis]

Carbon dioxide

124-38-9

3-FLUORO-N-METHYLANILINE

1978-37-6

N,N-DIMETHYL-3-FLUOROANILINE

2107-43-9

The general procedure for the synthesis of 3-fluoro-N,N-dimethylaniline from carbon dioxide and 3-fluoro-N-methylaniline was as follows: the methylation of various secondary amines was carried out using the general method Example II. The specific operating conditions were as follows: the substituted aromatic amines (1.0 mmol), [Ru(Triphos)(TMM)] (2.5 mol%), and HNTf2 (5 mol%) were dissolved in THF (2 mL), and reacted at 150 °C under a CO2/H2 (20/60 bar) atmosphere. The reaction time and yield data are detailed in Table II below.The reaction times and corresponding yields for different amine substrates are listed in Table II.

[References]

[1] Patent: WO2015/753, 2015, A1. Location in patent: Page/Page column 8-9
[2] Chemical Science, 2013, vol. 4, # 5, p. 2127 - 2131
[3] Angewandte Chemie - International Edition, 2013, vol. 52, # 36, p. 9554 - 9557
[4] Angew. Chem., 2013, vol. 125, # 36, p. 9733 - 9736
[5] Patent: EP2821397, 2015, A1. Location in patent: Paragraph 0039; 0041
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