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116632-14-5

116632-14-5 Structure

116632-14-5 Structure
IdentificationBack Directory
[Name]

2-Amino-3-iodonaphthalene
[CAS]

116632-14-5
[Synonyms]

3-iodonaphthalen-2-amine
2-Naphthalenamine,3-iodo-
2-Amino-3-iodonaphthalene
[Molecular Formula]

C10H8IN
[MDL Number]

MFCD12028563
[MOL File]

116632-14-5.mol
[Molecular Weight]

269.08
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[Appearance]

White to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362+P364-P403+P233-P501c
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

2-Amino-3-iodonaphthalene(116632-14-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-IODO-3-NITRONAPHTHALENE

102153-71-9

2-Amino-3-iodonaphthalene

116632-14-5

In a 250 mL three-necked flask, under nitrogen atmosphere, 0.04 mol 2-iodo-3-nitronaphthalene (Intermediate 2-1) and 0.08 mol SnCl2 were added and dissolved in 100 mL of ethanol. The mixture was heated to reflux and reacted for 6 hours. The progress of the reaction was monitored by thin layer chromatography (TLC) and the reaction was stopped after confirming the complete consumption of intermediate 2-1. The reaction solution was allowed to cool to room temperature and filtered. The filtrate was rotary evaporated under reduced pressure until no fraction evaporated. Finally, the intermediate 2-2 (3-iodonaphthalen-2-amine) was purified by neutral silica gel column chromatography and analyzed by high performance liquid chromatography (HPLC) with 99.1% purity and 75.9% yield.

[References]

[1] Tetrahedron Letters, 2000, vol. 41, # 16, p. 2781 - 2785
[2] Journal of Organic Chemistry, 2001, vol. 66, # 13, p. 4525 - 4542
[3] Patent: CN107868051, 2018, A. Location in patent: Paragraph 0104; 0106
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