ChemicalBook--->CAS DataBase List--->2368-80-1

2368-80-1

2368-80-1 Structure

2368-80-1 Structure
IdentificationMore
[Name]

2-Fluorophenylhydrazine
[CAS]

2368-80-1
[Synonyms]

1-(2-fluorophenyl)hydrazine
2-FLUOROPHENYLHYDRAZINE
ASINEX-REAG BAS 05500094
2-Fluoropherylhydrazine
o-Fluorophenylhydrazine
[EINECS(EC#)]

220-886-4
[Molecular Formula]

C6H7FN2
[MDL Number]

MFCD00041260
[Molecular Weight]

126.13
[MOL File]

2368-80-1.mol
Chemical PropertiesBack Directory
[Melting point ]

47°C
[Boiling point ]

76-79°C/3mm
[density ]

1.257±0.06 g/cm3(Predicted)
[storage temp. ]

Keep Cold
[form ]

solid
[pka]

4.73±0.10(Predicted)
[color ]

White to tan
[CAS DataBase Reference]

2368-80-1(CAS DataBase Reference)
[EPA Substance Registry System]

2368-80-1(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[TSCA ]

TSCA listed
[HS Code ]

2928009090
Hazard InformationBack Directory
[Synthesis]

2-Fluoroaniline

348-54-9

2-Fluorophenylhydrazine

2368-80-1

General procedure for the synthesis of 2-fluorophenylhydrazine from o-fluoroaniline: 500 g of o-fluoroaniline and 1500 mL of 37% concentrated hydrochloric acid were added to a 10 L three-necked flask and cooled to 2 °C using an ice-salt bath. 857 g of 35% aqueous sodium nitrite solution was added slowly and dropwise under stirring, and the reaction temperature was controlled to be maintained at 0 to 5 °C for 1.5 hours. Subsequently, 730 mL of 37% concentrated hydrochloric acid, 730 mL of water, and 480 g of zinc powder were added to the reaction solution, and the reaction temperature was maintained at 18 °C until the reaction was complete and the reaction solution turned off-white. Then, 30% sodium hydroxide solution was slowly added to adjust the pH of the reaction solution to 10.5, and this process took about 2 hours, and then crystals were precipitated, and 295 g of 2-fluorophenylhydrazine crude product was obtained by filtration. Purification step: 295 g of 2-fluorophenylhydrazine crude was dissolved in 5900 mL of water, heated to 60 ℃ to make it completely dissolved, and added appropriate amount of activated carbon to decolorize for 20 minutes, and then thermo-filtered to obtain a colorless filtrate. The filtrate was allowed to stand for 5 hours and then continued to stand for 2 hours, and the precipitated crystal precipitate was collected by filtration to finally obtain 238g of purified 2-fluorophenylhydrazine.

[References]

[1] Journal of Medicinal Chemistry, 1991, vol. 34, # 9, p. 2892 - 2898
[2] Chemistry - An Asian Journal, 2015, vol. 10, # 8, p. 1618 - 1621
[3] Molecules, 2016, vol. 21, # 11,
[4] Patent: CN106518723, 2017, A. Location in patent: Paragraph 0037-0046
[5] Patent: CN106518714, 2017, A. Location in patent: Paragraph 0017 - 0023
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